Pharmaceutical use of substituted amides

ABSTRACT

The use of substituted amides for modulating the activity of 11β-hydroxysteroid dehydrogenase type 1 (11βHSD1) and the use of these compounds as pharmaceutical compositions, are described. Also a novel class of substituted amides, their use in therapy, pharmaceutical compositions comprising the compounds, as well as their use in the manufacture of medicaments are described. The present compounds are modulators and more specifically inhibitors of the activity of 11βHSD1 and may be useful in the treatment, prevention and/or prophylaxis of a range of medical disorders where a decreased intracellular concentration of active glucocorticoid is desirable.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a continuation of U.S. application Ser. No.11/265,794 filed Oct. 11, 2005, which is a continuation of InternationalApplication No. PCT/DK2004/000250, filed Apr. 6, 2004, which claimspriority from Danish Patent Application Nos. PA 2003 00565, filed Apr.11, 2003; PA 2003 00972, filed Jun. 27, 2003; PA 2003 00988, filed Jun.30, 2003; PA 2003 00989, filed Jun. 30, 2003; PA 2003 00990, filed Jun.30, 2003; PA 2003 00998, filed Jul. 2, 2003; PA 2003 01910, filed Dec.22, 2003; and PA 2004 00009, filed Jan. 6, 2004; and U.S. PatentApplication Nos. 60/467,800, filed May 2, 2003; 60/486,095, filed Jul.10, 2003; 60/486,097, filed Jul. 10, 2003; 60/486,094, filed Jul. 10,2003; 60/486,078, filed Jul. 10, 2003; 60/486,098, filed Jul. 10, 2003;and 60/537,099, filed Jan. 16, 2004.

FIELD OF INVENTION

The present invention relates to use of substituted amides andpharmaceutical compositions comprising the compounds for treatingdisorders where it is desirable to modulate the activity of11β-hydroxysteroid dehydrogenase type 1 (11βHSD1).

The present invention also relates to novel substituted amides, to theiruse in therapy, to pharmaceutical compositions comprising the compounds,to the use of said compounds in the manufacture of medicaments, and totherapeutic methods comprising the administration of said compounds. Thepresent compounds modulate the activity of 11β-hydroxysteroiddehydrogenase type 1 (11βHSD1) and are accordingly useful in thetreatment of diseases in which such a modulation is beneficial, such asthe metabolic syndrome.

BACKGROUND OF THE INVENTION

The metabolic syndrome is a major global health problem. In the US, theprevalence in the adult population is currently estimated to beapproximately 25%, and it continues to increase both in the US andworldwide. The metabolic syndrome is characterised by a combination ofinsulin resistance, dyslipidemia, obesity and hypertension leading toincreased morbidity and mortality of cardiovascular diseases. Peoplewith the metabolic syndrome are at increased risk of developing franktype 2 diabetes, the prevalence of which is equally escalating.

In type 2 diabetes, obesity and dyslipidemia are also highly prevalentand around 70% of people with type 2 diabetes additionally havehypertension once again leading to increased mortality of cardiovasculardiseases.

In the clinical setting, it has long been known that glucocorticoids areable to induce all of the cardinal features of the metabolic syndromeand type 2 diabetes.

11β-hydroxysteroid dehydrogenase type 1 (11βHSD1) catalyses the localgeneration of active glucocorticoid in several tissues and organsincluding predominantly the liver and adipose tissue, but also e.g.skeletal muscle, bone, pancreas, endothelium, ocular tissue and certainparts of the central nervous system. Thus, 11βHSD1 serves as a localregulator of glucocorticoid actions in the tissues and organs where itis expressed (Tannin et al., J. Biol. Chem., 266, 16653 (1991); Bujalskaet al., Endocrinology, 140, 3188 (1999); Whorwood et al., J ClinEndocrinol Metab., 86, 2296 (2001); Cooper et al., Bone, 27, 375 (2000);Davani et al., J. Biol. Chem., 275, 34841 (2000); Brem et al.,Hypertension, 31, 459 (1998); Rauz et al., Invest. Ophthalmol. Vis.Sci., 42, 2037 (2001); Moisan et al., Endocrinology, 127, 1450 (1990)).

The role of 11βHSD1 in the metabolic syndrome and type 2 diabetes issupported by several lines of evidence. In humans, treatment with thenon-specific 11βHSD1 inhibitor carbenoxolone improves insulinsensitivity in lean healthy volunteers and people with type 2 diabetes.Likewise, 11βHSD1 knock-out mice are resistant to insulin resistanceinduced by obesity and stress. Additionally, the knock-out mice presentwith an anti-atherogenic lipid profile of decreased VLDL triglyceridesand increased HDL-cholesterol. Conversely, mice that overexpress 11βHSD1in adipocytes develop insulin resistance, hyperlipidemia and visceralobesity, a phenotype that resembles the human metabolic syndrome(Andrews et al., J. Clin. Endocrinol. Metab., 88, 285 (2003); Walker etal., J. Clin. Endocrinol. Metab., 80, 3155 (1995); Morton et al., J.Biol. Chem., 276, 41293 (2001); Kotelevtsev et al., Proc. Natl. Acad.Sci. USA, 94, 14924 (1997); Masuzaki et al., Science, 294, 2166 (2001)).

The more mechanistic aspects of 11βHSD1 modulation and therebymodulation of intracellular levels of active glucocorticoid have beeninvestigated in several rodent models and different cellular systems.11βHSD1 promotes the features of the metabolic syndrome by increasinghepatic expression of the rate-limiting enzymes in gluconeogenesis,namely phosphoenolpyuvate carboxykinase and glucose-6-phosphatase,promoting the differentiation of preadipocytes into adipocytes thusfacilitating obesity, directly and indirectly stimulating hepatic VLDLsecretion, decreasing hepatic LDL uptake and increasing vesselcontractility (Kotelevtsev et al., Proc. Natl. Acad. Sci. USA, 94, 14924(1997); Morton et al., J. Biol. Chem. 276, 41293 (2001); Bujalska etal., Endocrinology, 140, 3188 (1999); Souness et al., Steroids, 67, 195(2002), Brindley & Salter, Prog. Lipid Res., 30, 349 (1991)).

WO 01/90090, WO 01/90091, WO 01/90092, WO 01/90093 and WO 01/90094discloses various thiazol-sulfonamides as inhibitors of the human11β-hydroxysteroid dehydrogenase type 1 enzyme, and further states thatsaid compounds may be useful in treating diabetes, obesity, glaucoma,osteoporosis, cognitive disorders, immune disorders and depression.

We have now found substituted amides that modulate the activity of11βHSD1 leading to altered intracellular concentrations of activeglucocorticoid. More specifically, the present compounds inhibit theactivity of 11βHSD1 leading to decreased intracellular concentrations ofactive glucocorticoid. Thus, the present compounds can be used to treatdisorders where a decreased level of active intracellular glucocorticoidis desirable, such as e.g. the metabolic syndrome, type 2 diabetes,impaired glucose tolerance (IGT), impaired fasting glucose (IFG),dyslipidemia, obesity, hypertension, diabetic late complications,cardiovascular diseases, arteriosclerosis, atherosclerosis, myopathy,muscle wasting, osteoporosis, neurodegenerative and psychiatricdisorders, and adverse effects of treatment or therapy withglucocorticoid receptor agonists.

One object of the present invention is to provide compounds,pharmaceutical compositions and use of compounds that modulate theactivity of 11βHSD1.

DEFINITIONS

In the following structural formulas and throughout the presentspecification, the following terms have the indicated meaning:

The term “halo” includes fluorine, chlorine, bromine, and iodine.

The term “trihalomethyl” includes trifluoromethyl, trichloromethyl,tribromomethyl, and triiodomethyl.

The term “trihalomethoxy” includes trifluorometoxy, trichlorometoxy,tribromometoxy, and triiodometoxy.

The term “alkyl” includes C₁-C₈ straight chain saturated and methylenealiphatic hydrocarbon groups, C₃-C₈ branched saturated hydrocarbongroups having the specified number of carbon atoms. For example, thisdefinition shall include but is not limited to methyl (Me), ethyl (Et),propyl (Pr), butyl (Bu), pentyl, hexyl, isopropyl (i-Pr), isobutyl(i-Bu), tert-butyl (t-Bu), secbutyl (s-Bu), isopentyl, neopentyl, andthe like.

The term “alkenyl” includes C₂-C₆ straight chain unsaturated aliphatichydrocarbon groups and branched C₃-C₆ unsaturated aliphatic hydrocarbongroups having the specified number of carbon atoms. For example, thisdefinition shall include but is not limited to ethenyl, propenyl,butenyl, pentenyl, hexenyl, methylpropenyl, methylbutenyl and the like.

The term “alkynyl” includes C₂-C₆ straight chain unsaturated aliphatichydrocarbon groups and C₄-C₆ branched unsaturated aliphatic hydrocarbongroups having the specified number of carbon atoms. For example, thisdefinition shall include but is not limited to ethynyl, propynyl,butynyl, pentynyl, hexynyl, methylbutynyl, and the like.

The term “saturated or partially saturated cyclic, bicyclic or tricyclicring system” represents but are not limit to aziridinyl, azepanyl,azocanyl, pyrrolinyl, pyrrolidinyl, 2-imidazolinyl, imidazolidinyl,2-pyrazolinyl, morpholinyl, piperidinyl, thiomorpholinyl, piperazinyl,phthalimide, 1,2,3,4-tetrahydro-quinolinyl,1,2,3,4-tetrahydro-isoquinolinyl, 1,2,3,4-tetrahydro-quinoxalinyl,indolinyl, 1,6-aza-bicyclo[3.2.1]octane, 2-aza-bicyclo[4.1.1]octane,2-aza-bicyclo[3.2.1]octanyl, 7-aza-bicyclo[4.1.1]octanyl,9-aza-bicyclo[3.3.2]decanyl, 4-aza-tricyclo[4.3.1.1^(3,8)]undecanyl,9-aza-tricyclo[3.3.2.0^(3,7)]decanyl.

The term “saturated or partially saturated cyclic ring system”represents but are not limited to cyclopropyl, cyclobutyl, cyclopentyl,cyclohexyl, cyclobutenyl, cyclopentenyl, cyclohexenyl, cycloheptenyl,cyclooctenyl, cyclononenyl, cyclodecenyl, tetrahydrofuranyl ortetrahydropyranyl.

The term “saturated or partially saturated aromatic ring system”represents but are not limited to cyclopentyl, cyclohexyl, cyclobutenyl,cyclopentenyl, cyclohexenyl, cycloheptenyl, cyclooctenyl, cyclononenyl,cyclodecenyl, tetrahydrofuranyl, tetrahydropyranyl, phenyl, pyridyl orpyrimidinyl.

The term “cycloalkyl” (e.g. cyclopropyl, cyclobutyl, cyclopentyl,cyclohexyl, cycloheptyl, cyclooctyl, cyclononyl, cyclodecyl,bicyclo[3.2.1]octyl, spiro[4.5]decyl, norpinyl, norbonyl, norcaryl,adamantyl and the like) represents a saturated, mono-, bi-, tri- orspirocarbocyclic group having the specified number of carbon atoms.

The term “cycloalkylalkyl” (e.g. cyclopropylmethyl, cyclobutylethyl,adamantylmethyl and the like) represents a cycloalkyl group as definedabove attached through an alkyl group having the indicated number ofcarbon atoms or substituted alkyl group as defined above.

The term “cycloalkenyl” (e.g. cyclobutenyl, cyclopentenyl, cyclohexenyl,cycloheptenyl, cyclooctenyl, cyclononenyl, cyclodecenyl and the like)represents a partially saturated, mono-, bi-, tri- or spirocarbocyclicgroup having the specified number of carbon atoms.

The term “cycloalkylcarbonyl” (e.g. cyclopropylcarbonyl,cyclohexylcarbonyl) represents an cycloalkyl group as defined abovehaving the indicated number of carbon atoms attached through a carbonylgroup.

The term “hetcycloalkylcarbonyl” (e.g. 1-piperidin-4-yl-carbonyl,1-(1,2,3,4-tetrahydroisoquinolin-6-yl)carbonyl) represents anhetcycloalkyl group as defined above having the indicated number ofcarbon atoms attached through a carbonyl group.

The term “cycloalkylalkylcarbonyl” (e.g. cyclohexylmethylcarbonyl,cycloheptylethylcarbonyl and the like) represents a cycloalkyl group asdefined above attached through an alkyl group having the indicatednumber of carbon atoms or substituted alkyl group as defined above.

The term “hetcycloalkyl” (tetrahydrofuranyl, tetrahydropyranyl,tertahydrothiopyranyl, piperidine, pyridzine and the like) represents asaturated mono-, bi-, tri- or spirocarbocyclic group having thespecified number of carbon atoms and one or two additional heteroatomsor groups selected from nitrogen, oxygen, sulphur, SO or SO₂.

The term “hetcycloalkylalkyl” (e.g. tetrahydrofuranylmethyl,tetrahydropyranylethyl, tertahydrothiopyranylmethyl, and the like)represents a hetcycloalkyl group as defined above attached through analkyl group having the indicated number of carbon atoms or substitutedalkyl group as defined above.

The term “alkyloxy” (e.g. methoxy, ethoxy, propyloxy, allyloxy,cyclohexyloxy) represents an alkyl group as defined above having theindicated number of carbon atoms attached through an oxygen bridge.

The term “alkyloxyalkyl” (e.g. methyloxymethyl and the like) representsan alkyloxy group as defined above attached through an “alkyl” group.

The term “aryloxyhetaryl” (e.g. 2-phenoxy-pyridyl and the like)represents an aryloxy group as defined below attached through a“hetaryl” group.

The term “aryloxy” (e.g. phenoxy, naphthyloxy and the like) representsan aryl group as defined below attached through an oxygen bridge.

The term “hetaryloxy” (e.g. 2-pyridyloxy and the like) represents ahetaryl group as defined below attached through an oxygen bridge.

The term “arylalkyloxy” (e.g. phenethyloxy, naphthylmethyloxy and thelike) represents an arylalkyl group as defined below attached through anoxygen bridge.

The term “hetarylalkyloxy” (e.g. 2-pyridylmethyloxy and the like)represents a hetarylalkyl group as defined below attached through anoxygen bridge.

The term “alkyloxycarbonyl” (e.g. methylformiat, ethylformiat and thelike) represents an alkyloxy group as defined above attached through acarbonyl group.

The term “aryloxycarbonyl” (e.g. phenylformiat, 2-thiazolylformiat andthe like) represents an aryloxy group as defined above attached througha carbonyl group.

The term “arylalkyloxycarbonyl” (e.g. benzylformiat, phenyletylformiatand the like) represents an “arylalkyloxy” group as defined aboveattached through a carbonyl group.

The term “alkylthio” (e.g. methylthio, ethylthio and the like)represents an alkyl group as defined above attached through a sulphurbridge.

The term “arylthio” (e.g. benzenthiol, naphthylthiol and the like)represents an aryl group as defined below attached through a sulphurbridge.

The term “hetarylthio” (e.g. pyridine-2-thiol, thiazole-2-thiol and thelike) represents an hetaryl group as defined below attached through asulphur bridge.

The term “arylthioalkyl” (e.g. methylsulfanyl benzene, ethylsulfanylnaphthalene and the like) represents an arylthio group as defined belowattached through an alkyl group having the indicated number of carbonatoms.

The term “hetarylthioalkyl” (e.g. 2-methylsulfanyl-pyridine,1-ethylsulfanyl-isoquinoline and the like) represents a hetarylthiogroup as defined below attached through an alkyl group having theindicated number of carbon atoms.

The term “hetaryloxyaryl” (e.g. 1-phenoxy-isoquinolyl, 2-phenoxypyridyland the like) represents a hetaryloxy group as defined above attachedthrough an “aryl” group as defined below.

The term “hetaryloxyhetaryl” (e.g. 1-(2-pyridyloxy-isoquinoline),2-(imidazol-2-yloxypyridine) and the like) represents a hetaryloxy groupas defined above attached through a “hetaryl” group as defined below.

The term “aryloxyalkyl” (e.g. phenoxymethyl, naphthyloxyethyl and thelike) represents an aryloxy group as defined above attached through an“alkyl” group having the indicated number of carbon atoms.

The term “aryloxyaryl” (e.g. 1-phenoxy-naphthalene, phenyloxyphenyl andthe like) represents an aryloxy group as defined above attached throughan “aryl” group as defined below.

The term “arylalkyloxyalkyl” (e.g. ethoxymethyl-benzene,2-methoxymethylnaphthalene and the like) represents an arylalkyloxygroup as defined above attached through an “alkyl” group having theindicated number of carbon atoms.

The term “hetaryloxyalkyl” (e.g. 2-pyridyloxymethyl, 2-quinolyloxyethyland the like) represents a hetaryloxy group as defined above attachedthrough an “alkyl” group having the indicated number of carbon atoms.

The term “hetarylalkyloxyalkyl” (e.g. 4-methoxymethyl-pyrimidine,2-methoxymethylquinoline and the like) represents a hetarylalkyloxygroup as defined above attached through an “alkyl” group having theindicated number of carbon atoms.

The term “arylalkyl” (e.g. benzyl, phenylethyl, 3-phenylpropyl,1-naphtylmethyl, 2-(1-naphtyl)ethyl and the like) represents an arylgroup as defined below attached through an alkyl having the indicatednumber of carbon atoms or substituted alkyl group as defined above.

The term “hetarylalkyl” or “hetaralkyl” (e.g. (2-furyl)methyl,(3-furyl)methyl, (2-thienyl)methyl, (3-thienyl)methyl,(2-pyridyl)methyl, 1-methyl-1-(2-pyrimidyl)ethyl and the like)represents a hetaryl group as defined below attached through an alkylhaving the indicated number of carbon atoms or substituted alkyl groupas defined above.

The term “alkylcarbonyl” (e.g. octylcarbonyl, pentylcarbonyl,3-hexenylcarbonyl) represents an alkyl group as defined above having theindicated number of carbon atoms attached through a carbonyl group.

The term “arylcarbonyl” (e.g. benzoyl) represents an aryl group asdefined below attached through a carbonyl group.

The term “hetarylcarbonyl” (e.g. 2-thiophenylcarbonyl,3-methoxy-anthrylcarbonyl, oxazolylcarbonyl and the like) represents ahetaryl group as defined below attached through a carbonyl group.

The term “carbonylalkyl” (e.g. acetyl and the like) represents acarbonyl group attached through alkyl group as defined above having theindicated number of carbon atoms.

The term “alkylcarbonylalkyl” (e.g. propan-2-one,4,4-dimethyl-pentan-2-one and the like) represents an alkylcarbonylgroup as defined above attached through an alkyl group as defined abovehaving the indicated number of carbon atoms.

The term “arylcarbonylalkyl” (e.g. 1-phenyl-propan-1-one,1-(3-chloro-phenyl)-2-methylbutan-1-one and the like) represents aarylcarbonyl group as defined above attached through an alkyl group asdefined above having the indicated number of carbon atoms.

The term “hetarylcarbonylalkyl” (e.g. 1-pyridin-2-yl-propan-1-one,1-(1-H-imidazol-2-yl)propan-1-one and the like) represents ahetarylcarbonyl group as defined above attached through an alkyl groupas defined above having the indicated number of carbon atoms.

The term “arylalkylcarbonyl” (e.g. phenylpropylcarbonyl,phenylethylcarbonyl and the like) represents an arylalkyl group asdefined above having the indicated number of carbon atoms attachedthrough a carbonyl group.

The term “hetarylalkylcarbonyl” (e.g. imidazolylpentylcarbonyl and thelike) represents a hetarylalkyl group as defined above wherein the alkylgroup is in turn attached through a carbonyl.

The term “alkylcarbonylamino” (e.g. methylcarbonylamino,cyclopentylcarbonylaminomethyl, methylcarbonylaminophenyl) represents an“alkylcarbonyl” group as defined above wherein the carbonyl is in turnattached through the nitrogen atom of an amino group. The nitrogen atommay itself be substituted with an alkyl or aryl group.

The term “alkylcarbonylaminoalkyl” (e.g. N-propyl-acetamide,N-butyl-propionamide and the like) represents an “alkylcarbonylamino”group attached through an alkyl group as defined above having theindicated number of carbon atoms.

The term “arylalkylcarbonylamino” (e.g. phenylacetamide,3phenyl-propionamide and the like) represents an “arylalkylcarbonyl”group as defined above attached through an amino group.

The term “arylalkylcarbonylaminoalkyl” (e.g. N-ethyl-phenylacetamide,N-butyl-3-phenyl-propionamide and the like) represents an“arylalkylcarbonylamino” group attached through an alkyl group asdefined above having the indicated number of carbon atoms.

The term “arylcarbonylamino” (e.g. benzamide, naphthalene-1-carboxylicacid amide and the like) represents an “arylcarbonyl” group as definedabove attached through an amino group.

The term “arylcarbonylaminoalkyl” (e.g. N-propyl-benzamide,N-Butyl-naphthalene-1-carboxylic acid amide and the like) represents an“arylcarbonylamino” group attached through an alkyl group as definedabove having the indicated number of carbon atoms.

The term “alkylcarboxy” (e.g. heptylcarboxy, cyclopropylcarboxy,3-pentenylcarboxy) represents an alkylcarbonyl group as defined abovewherein the carbonyl is in turn attached through an oxygen bridge.

The term “arylcarboxy” (e.g. benzoic acid and the like) represents anarylcarbonyl group as defined above wherein the carbonyl is in turnattached through an oxygen bridge.

The term “alkylcarboxyalkyl” (e.g. heptylcarboxymethyl, propylcarboxytert-butyl, 3-pentylcarboxyethyl) represents an

The term “arylalkylcarboxy” (e.g. benzylcarboxy, phenylpropylcarboxy andthe like) represents an arylalkylcarbonyl group as defined above whereinthe carbonyl is in turn attached through an oxygen bridge.

The term “arylalkylcarboxyalkyl” (e.g. benzylcarboxymethyl,phenylpropylcarboxypropyl and the like) represents an arylalkylcarboxygroup as defined above wherein the carboxy group is in turn attachedthrough an alkyl group as defined above having the indicated number ofcarbon atoms.

The term “hetarylcarboxy” (e.g. pyridine-2-carboxylic acid and the like)represents a hetarylcarbonyl group as defined above wherein the carbonylis in turn attached through an oxygen bridge.

The term “hetarylalkylcarboxy” (e.g. (1-H-imidazol-2-yl)-acetic acid,3-pyrimidin-2-yl-propionic acid and the like) represents ahetarylalkylcarbonyl group as defined above wherein the carbonyl is inturn attached through an oxygen bridge.

The term “aryl” includes but is not limited to a carbocyclic aromaticring system being either monocyclic, bicyclic, or polycyclic, such asphenyl, biphenyl, naphthyl, anthracenyl, phenanthrenyl, fluorenyl,indenyl, pentalenyl, azulenyl, biphenylenyl and the like. Aryl is alsointended to include the partially hydrogenated derivatives of thecarbocyclic aromatic systems enumerated above. Non-limiting examples ofsuch partially hydrogenated derivatives are 1,2,3,4-tetrahydronaphthyl,1,4-dihydronaphthyl and the like.

The term “aryl1” includes phenyl, biphenyl, naphthyl, anthracenyl,phenanthrenyl, and fluorenyl.

The term “aryl2” includes phenyl, biphenyl, and naphthyl.

The term “hetaryl” includes but is not limited to pyrrolyl (2-pyrrolyl),pyrazolyl (3-pyrazolyl), imidazolyl (1-imidazolyl, 2-imidazolyl,4-imidazolyl, 5-imidazolyl), triazolyl (1,2,3-triazol-1-yl,1,2,3-triazol-2-yl 1,2,3-triazol-4-yl, 1,2,4-triazol-3-yl), oxazolyl(2-oxazolyl, 4-oxazolyl, 5-oxazolyl), isoxazolyl (3-isoxazolyl,4-isoxazolyl, 5-isoxazolyl), thiazolyl (2-thiazolyl, 4-thiazolyl,5-thiazolyl), thiophenyl (2-thiophenyl, 3-thiophenyl, 4-thiophenyl,5-thiophenyl), furanyl (2-furanyl, 3-furanyl, 4-furanyl, 5-furanyl),pyridyl (2-pyridyl, 3-pyridyl, 4-pyridyl, 5-pyridyl), 5-tetrazolyl,pyrimidinyl (2-pyrimidinyl, 4-pyrimidinyl, 5-pyrimidinyl,6-pyrimidinyl), pyrazinyl, pyridazinyl (3-pyridazinyl, 4-pyridazinyl,5-pyridazinyl), quinolyl (2-quinolyl, 3-quinolyl, 4-quinolyl,5-quinolyl, 6-quinolyl, 7-quinolyl, 8-quinolyl), isoquinolyl(1-isoquinolyl, 3-isoquinolyl, 4-isoquinolyl, 5-isoquinolyl,6-isoquinolyl, 7-isoquinolyl, 8-isoquinolyl), benzo[b]furanyl(2-benzo[b]furanyl, 3-benzo[b]furanyl, 4-benzo[b]furanyl,5-benzo[b]furanyl, 6-benzo[b]furanyl, 7-benzo[b]furanyl),2,3-dihydro-benzo[b]furanyl (2-(2,3-dihydro-benzo[b]furanyl),3-(2,3-dihydro-benzo[b]furanyl), 4-(2,3-dihydro-benzo[b]furanyl),5-(2,3-dihydro-benzo-[b]furanyl), 6-(2,3-dihydro-benzo-[b]furanyl),7-(2,3-dihydro-benzo[b]furanyl)), benzo[b]thiophenyl(2-benzo[b]thiophenyl, 3-benzo[b]thiophenyl, 4-benzo[b]thiophenyl,5-benzo[b]thiophenyl, 6-benzo[b]thiophenyl, 7-benzo[b]thiophenyl),2,3-dihydro-benzo[b]thiophenyl (2-(2,3-dihydro-benzo[b]thiophenyl),3-(2,3-dihydro-benzo[b]thiophenyl), 4-(2,3-dihydro-benzo[b]thiophenyl),5-(2,3-dihydro-benzo[b]thiophenyl), 6-(2,3-dihydro-benzo[b]thiophenyl),7-(2,3-dihydro-benzo[b]thiophenyl)),4,5,6,7-tetrahydro-benzo[b]thiophenyl(2-(4,5,6,7-tetrahydro-benzo[b]thiophenyl),3-(4,5,6,7-tetrahydro-benzo[b]thiophenyl),4-(4,5,6,7-tetrahydro-benzo[b]thiophenyl),5-(4,5,6,7-tetrahydro-benzo[b]thiophenyl),6-(4,5,6,7-tetrahydro-benzo[b]thiophenyl),7-(4,5,6,7-tetrahydro-benzo[b]thiophenyl)), thieno[2,3-b]thiophenyl,4,5,6,7-tetrahydro-thieno[2,3-c]pyridyl(4-(4,5,6,7-tetrahydro-thieno[2,3-c]pyridyl),5-4,5,6,7-tetrahydro-thieno[2,3-c]pyridyl),6-(4,5,6,7-tetrahydro-thieno[2,3-c]pyridyl),7-(4,5,6,7-tetrahydro-thieno[2,3-c]pyridyl)), indolyl (1-indolyl,2-indolyl, 3-indolyl, 4-indolyl, 5-indolyl, 6-indolyl, 7-indolyl),isoindolyl (1-isoindolyl, 2-isoindolyl, 3-isoindolyl, 4-isoindolyl,5-isoindolyl, 6-isoindolyl, 7-isoindolyl), 1,3-dihydro-isoindolyl(1-(1,3-dihydro-isoindolyl), 2-(1,3-dihydro-isoindolyl),3-(1,3-dihydro-isoindolyl), 4-(1,3-dihydro-isoindolyl),5-(1,3-dihydro-isoindolyl), 6-(1,3-dihydro-isoindolyl),7-(1,3-dihydro-isoindolyl)), indazole (1-indazolyl, 3-indazolyl,4-indazolyl, 5-indazolyl, 6-indazolyl, 7-indazolyl), benzimidazolyl(1-benzimidazolyl, 2-benzimidazolyl, 4-benzimidazolyl, 5-benzimidazolyl,6-benzimidazolyl, 7-benzimidazolyl, 8-benzimidazolyl), benzoxazolyl(1-benz-oxazolyl, 2-benzoxazolyl), benzothiazolyl (1-benzothiazolyl,2-benzothiazolyl, 4-benzothiazolyl, 5-benzothiazolyl, 6-benzothiazolyl,7-benzothiazolyl), benzo-[1,2,5]oxadiazolyl, (4-benzo[1,2,5]oxadiazole,5-benzo[1,2,5]oxadiazole), carbazolyl (1-carbazolyl, 2-carbazolyl,3-carbazolyl, 4-carbazolyl), piperidinyl (2-piperidinyl, 3-piperidinyl,4-piperidinyl), pyrrolidinyl (1-pyrrolidinyl, 2-pyrrolidinyl,3-pyrrolidinyl).

The term “alkylSO_(m)” (e.g. ethylsulfonyl, ethylsulfinyl and the like)represents an alkyl group as defined above, wherein the alkyl group isin turn attached through a sulphur bridge wherein the sulphur issubstituted with m oxygen atoms.

The term “arylSO_(m)” (e.g. phenylsulfinyl, naphthyl-2-sulfonyl and thelike) represents an aryl group as defined above, wherein the aryl groupis in turn attached through a sulphur bridge wherein the sulphur issubstituted with m oxygen atoms.

The term “hetarylSO_(m)” (e.g. thiazol-2-sulfinyl, pyridine-2-sulfonyland the like) represents a hetaryl group as defined above, wherein thehetaryl group is in turn attached through a sulphur bridge wherein thesulphur is substituted with m oxygen atoms.

With respect to formula I and II, the term “NR⁴R⁵carbonylalkyl” (e.g.N,N-dimethyl-propionamide, N-isopropyl-N-methyl-propionamide and thelike) represents NR⁴R⁵ substituted by a carbonylalkyl group as definedabove.

With respect to formula I and II, the term “alkylR⁶alkyl” (e.g.2-ethoxymethyl, N-ethyl-N-methy amine, methyl-propyl-amide,ethanesulfonic acid methylamide and the like) represents an alkyl groupas defined above, substituted by R⁶, which is substituted by an alkylgroup as defined above.

With respect to formula I and II, the term “arylR⁶alkyl” (e.g.ethoxy-benzene, N-ethyl-N-methyl-phenyl-amine, N-ethyl-benzamide,N-isobutyl-benzenesulfonamide and the like) represents an aryl group asdefined above, substituted by R⁶, which is substituted by an alkyl groupas defined above.

With respect to formula I and II, the term “arylalkylR⁶alkyl” (e.g.benzyloxymethyl, N-ethyl-N-methyl-benzyl-amine, N-ethyl-benzylamide andthe like) represents an arylalkyl group as defined above, substituted byR⁶, which is substituted by an alkyl group as defined above.

With respect to formula I and II, the term “hetarylR⁶alkyl” (e.g.2-ethoxy-1H-imidazol, ethyl-quinolin-2-yl-amine, thiazole-2-carboxylicacid, methyl-propyl-amide, pyridine-3-sulfonic acid isobutyl-amide andthe like) represents a hetaryl group as defined above, substituted byR⁶, which is substituted by an alkyl group as defined above.

With respect to formula I and II, the term “arylcarbonylNR¹⁵” (e.g.N-benzyl-N-methyl-benzamide and the like) represents an arylcarbonylgroup as defined above, substituted by NR¹⁵.

With respect to formula I and II, the term “arylSO_(m)NR⁸” (e.g.N-methyl-benzenesulfonamide and the like) represents an aryl group asdefined above, wherein the aryl group is in turn attached through aSO_(m)NR⁸ group wherein the sulphur is substituted with m oxygen atomsand the nitrogen atom substituted by R⁸.

With respect to formula III, the term “alkylNR⁵alkyl” (e.g.N-ethyl-N-isobutyl-amine, N,N-dimethylamine and the like wherein theamino group (N) is substituted with R⁵ as defined below) represents analkylNR⁵ group as defined above attached through an “alkyl” group.

With respect to formula III, the term “arylalkylNR⁵alkyl” (e.g.N-benzyl-N-methyl-amine, N-phenethyl-N-ethyl-amine and the like whereinthe amino group (N) is substituted with R⁵ as defined below) representsan arylalkylNR⁵ group as defined above attached through an “alkyl”group.

Certain of the above defined terms may occur more than once in thestructural formulae, and upon such occurrence each term shall be definedindependently of the other.

The term “optionally substituted” as used herein means that the groupsin question are either unsubstituted or substituted with one or more ofthe substituents specified. When the groups in question are substitutedwith more than one substituent, the substituents may be the same ordifferent.

The term “treatment” is defined as the management and care of a patientfor the purpose of combating or alleviating the disease, condition ordisorder, and the term includes the administration of the activecompound to prevent the onset of the symptoms or complications, oralleviating the symptoms or complications, or eliminating the disease,condition, or disorder.

The term “pharmaceutically acceptable” is defined as being suitable foradministration to humans without adverse events.

The term “prodrug” is defined as a chemically modified form of theactive drug, said prodrug being administered to the patient andsubsequently being converted to the active drug. Techniques fordevelopment of prodrugs are well known in the art.

DETAILED DESCRIPTION OF THE INVENTION

In one aspect, the present invention provides the use of a substitutedamide, a prodrug thereof, or a salt thereof with a pharmaceuticallyacceptable acid or base, or any optical isomer or mixture of opticalisomers, including a racemic mixture, or any tautomeric forms for

a) modulation of the activity of 11βHSD1; or

b) inhibition of 11βHSD1,

in a patient in need thereof.

In another aspect, the present invention provides the use of asubstituted amide, a prodrug thereof, or a salt thereof with apharmaceutically acceptable acid or base, or any optical isomer ormixture of optical isomers, including a racemic mixture, or anytautomeric forms for the preparation of a pharmaceutical composition forthe treatment, prevention and/or prophylaxis of any disorder and diseasewhere it is desirable to

a) modulate the activity of 11βHSD1; or

b) inhibit 11βHSD1,

in a patient in need thereof.

In another embodiment, the invention provides the present use ofsubstituted amides, or a prodrug thereof of the general formula (I)

whereinR¹ is C₃-C₁₀cycloalkyl, C₃-C₁₀hetcycloalkyl, C₁-C₈alkyl, aryl, hetaryl,arylC₁-C₆alkyl or hetarylC₁-C₆alkyl, wherein the cycloalkyl,hetcycloalkyl, alkyl, arylalkyl and hetarylalkyl groups independentlyare optionally substituted with one or more of R⁴.R² is hydrogen, C₁-C₈alkyl, aryl, hetaryl, arylC₁-C₆alkyl,C₃-C₁₀cycloalkylC₁-C₆alkyl, C₁-C₆alkylcarboxyC₁-C₆alkyl wherein thealkyl, aryl and cycloalkyl groups independently are optionallysubstituted with one or more of R⁵; orR¹ and R² together with the nitrogen to which they are attached, areforming a saturated or partially saturated cyclic, bicyclic or tricyclicring system containing from 4 to 10 carbon atoms and from 0 to 2additional heteroatoms selected from nitrogen, oxygen or sulphur, thering system optionally being substituted with at least one ofC₁-C₈alkyl, aryl, hetaryl, arylC₁-C₆alkyl, hetarylC₁-C₆alkyl, hydroxy,oxo, cyano, C₁-C₆alkyloxy, arylC₁-C₆alkyloxy, hetarylC₁-C₆alkyloxy,C₁-C₆alkyloxyC₁-C₆alkyl, C₁-C₆alkylcarbonyl, arylcarbonyl,hetarylcarbonyl, arylC₁-C₆alkylcarbonyl, hetarylC₁-C₆alkylcarbonyl,C₁-C₆alkylcarboxy, arylcarboxy or arylC₁-C₆alkylcarboxy wherein thealkyl and aryl groups independently are optionally substituted with oneor more of R¹⁴;R³ is C₁-C₈alkyl, C₁-C₆alkenyl, C₁-C₆alkynyl, C₃-C₁₀cycloalkyl,C₃-C₁₀hetcycloalkyl, aryl, hetaryl, arylC₁-C₆alkyl,C₁-C₆alkyloxyC₁-C₆alkyl, hetarylC₁-C₆alkyl, aryl-R⁶—C₁-C₆alkyl,hetaryl-R⁶—C₁-C₆alkyl or arylC₁-C₆alkyl-R⁶—C₁-C₆alkyl wherein the alkyl,cycloalkyl, hetcycloalkyl, alkenyl, alkynyl, aryl and hetaryl groupsindependently are optionally substituted with one or more of R⁷;R⁴ and R⁵ independently are hydrogen, hydroxy, oxo, cyano, halo,methylendioxo, NR⁸R⁹, C₁-C₈alkyl, C₁-C₆alkyloxy, trihalomethyl,trihalomethyloxy, C₃-C₁₀cycloalkyl, C₃-C₁₀hetcycloalkyl,C₃-C₁₀cycloalkenyl, aryl, hetaryl, hetarylSO_(n), arylC₁-C₆alkyloxy,hetarylC₁-C₆alkyloxy, C₁-C₆alkyl-R⁶—C₁-C₆alkyl,arylC₁-C₆alkyl-R⁶—C₁-C₆alkyl, C₁-C₆alkylcarbonyl, arylcarbonyl,arylC₁-C₆alkylcarbonyl, hetarylcarbonyl, hetarylC₁-C₆alkyl-carbonyl,C₁-C₆alkylSO_(n), C₁-C₆alkyl-carboxy, arylcarboxy, hetarylcarboxy,arylC₁-C₆alkylcarboxy or hetarylC₁-C₆alkylcarboxy wherein the alkyl,cycloalkyl, hetcycloalkyl, aryl and hetaryl groups independently areoptionally substituted with one or more of R¹⁵;R⁶ is oxygen, sulphur, SO_(n) or NR¹⁶;R⁷ is hydrogen, halo, hydroxy, cyano, nitro, COOR¹⁷, C₁-C₈alkyl,C₃-C₁₀cycloalkyl, C₃-C₁₀hetcycloalkyl, methylendioxo, trihalomethyl,trihalomethyloxy, aryl, arylC₁-C₆alkyl, C₁-C₆alkyloxy,C₁-C₆alkyloxyC₁-C₆alkyl, aryloxy, arylC₁-C₆alkyloxy, aryloxyC₁-C₆alkyl,arylC₁-C₆alkyloxyC₁-C₆alkyl, hetaryl, hetarylC₁-C₆alkyl, hetaryloxy,hetarylC₁-C₆alkyloxy, hetaryloxyC₁-C₆alkyl,hetarylC₁-C₆alkyl-oxyC₁-C₆alkyl, NR⁸R⁹, SO₂NR⁸R⁹,NR⁴R⁵carbonylC₁-C₆alkyl, arylthio, hetarylthio, R¹⁸carbonylNR⁸,arylSO_(n), hetarylSO_(n), R¹⁹SO_(m)NR⁸, arylthioC₁-C₆alkyl,hetarylthioC₁-C₆alkyl or arylC₁-C₆alkylR⁶C₁-C₆alkyl; wherein the aryland hetaryl groups independently are optionally substituted with one ormore R¹⁰;R⁸ and R⁹ independently are hydrogen, C₁-C₈alkyl, aryl, hetaryl,arylC₁-C₆alkyl or hetarylC₁-C₆alkyl wherein the alkyl, aryl and hetarylgroups independently are optionally substituted with one or more of R¹¹;orR⁸ and R⁹ together with the nitrogen to which they are attached, areforming a saturated or partially saturated cyclic, bicyclic or tricyclicring system containing from 4 to 10 carbon atoms and from 0 to 2additional heteroatoms selected from nitrogen, oxygen or sulfur, thering system optionally being substituted with at least one halo, cyano,C₁-C₈alkyl, aryl, hetaryl, arylC₁-C₆alkyl, hetarylC₁-C₆alkyl, hydroxy,oxo, C₁-C₆alkyloxy, arylC₁-C₆alkyloxy, hetarylC₁-C₆alkyloxy,C₁-C₆alkyloxyC₁-C₆alkyl, C₁-C₆alkyl-carbonyl, arylcarbonyl,hetarylcarbonyl, arylC₁-C₆alkylcarbonyl, hetarylC₁-C₆alkylcarbonyl,C₁-C₆alkylcarboxy, arylcarboxy, hetarylcarboxy, arylC₁-C₆alkylcarboxy orhetarylC₁-C₆alkylcarboxy;R¹⁰ and R¹¹ independently are hydrogen, hydroxy, oxo, halo, cyano,nitro, C₁-C₈alkyl, C₁-C₆alkyloxy, NR¹²R¹³, methylendioxo, trihalomethylor trihalomethyloxy;R¹² and R¹³ independently are hydrogen, C₁-C₈alkyl or arylC₁-C₆alkyl;R¹⁴ is hydrogen, halo, hydroxy, oxo, nitro, cyano, C₁-C₈alkyl,C₁-C₆alkyloxy or aryloxy;R¹⁵ is hydrogen, halo, hydroxy, oxo, nitro, cyano, CONR⁸R⁹ or COOR¹⁷;R¹⁶ is hydrogen, C₁-C₈alkyl, C₃-C₁₀cycloalkyl, C₃-C₁₀hetcycloalkyl,aryl, arylC₁-C₆alkyl, hetaryl, hetarylC₁-C₆alkyl, alkylcarbonyl,arylcarbonyl, arylC₁-C₆alkylcarbonyl, aryloxyC₁-C₆alkyl,hetaryloxyC₁-C₆alkyl, arylthioC₁-C₆alkyl or hetarylthioC₁-C₆alkyl;wherein the alkyl, cycloalkyl, hetcycloalkyl, aryl and hetaryl groupsindependently are optionally substituted with one or more of R¹⁰;R¹⁷ is hydrogen, C₁-C₈alkyl, aryl or arylC₁-C₆alkyl;R¹⁸ is C₁-C₆alkyl, C₂-C₆alkenyl, aryl, arylC₁-C₆alkyl, hetaryl,hetarylC₁-C₆alkyl, C₃-C₁₀cycloalkyl, C₃-C₁₀hetcycloalkyl, C₁-C₆alkyloxy,aryloxy, arylC₁-C₆alkyloxy, arylC₁-C₆alkyloxyC₁-C₆alkyl, hetaryloxy,hetarylC₁-C₆alkyloxy, hetarylC₁-C₆alkyloxyC₁-C₆alkyl or R⁸R⁹NC₁-C₆alkylwherein the alkyl, alkenyl, cycloalkyl, hetcycloalkyl, aryl and hetarylgroups are optionally substituted with R¹⁵;R¹⁹ is C₁-C₆alkyl, C₃-C₁₀cycloalkyl, C₃-C₁₀hetcycloalkyl, aryl,arylC₁-C₆alkyl, hetaryl, hetarylC₁-C₆alkyl;m is 1 or 2;n is 0, 1 or 2; ora salt thereof with a pharmaceutically acceptable acid or base, or anyoptical isomer or mixture of optical isomers, including a racemicmixture, or any tautomeric forms.

In another embodiment, the invention provides the present use of asubstituted amide, or a prodrug thereof of the above general formula (I)wherein

R¹ is C₃-C₁₀cycloalkyl, C₃-C₁₀hetcycloalkyl, C₁-C₈alkyl, aryl, hetaryl,arylC₁-C₆alkyl or hetarylC₁-C₆alkyl, wherein the cycloalkyl,hetcycloalkyl, alkyl, arylalkyl and hetarylalkyl groups independentlyare optionally substituted with one or more of R⁴;

R² is hydrogen, C₁-C₈alkyl, aryl, hetaryl, arylC₁-C₆alkyl,C₃-C₁₀cycloalkylC₁-C₆alkyl, C₁-C₆alkylcarboxyC₁-C₆alkyl wherein thealkyl, aryl and cycloalkyl groups independently are optionallysubstituted with one or more of R⁵; or

R¹ and R² are together with the nitrogen to which they are attached, areforming a saturated or partially saturated cyclic, bicyclic or tricyclicring system containing from 4 to 10 carbon atoms and from 0 to 2additional heteroatoms selected from nitrogen, oxygen or sulphur, thering system optionally being substituted with at least one ofC₁-C₈alkyl, aryl, hetaryl, arylC₁-C₆alkyl, hetarylC₁-C₆alkyl, hydroxy,oxo, cyano, C₁-C₆alkyloxy, arylC₁-C₆alkyloxy, hetarylC₁-C₆alkyloxy,C₁-C₆alkyloxyC₁-C₆alkyl, C₁-C₆alkylcarbonyl, arylcarbonyl,hetarylcarbonyl, arylC₁-C₆alkylcarbonyl, hetarylC₁-C₆alkylcarbonyl,C₁-C₆alkylcarboxy, arylcarboxy or arylC₁₋₆alkylcarboxy wherein the alkyland aryl groups independently are optionally substituted with one ormore of R¹⁴;

R³ is C₁-C₈alkyl, C₁-C₆alkenyl, C₁-C₆alkynyl, C₃-C₁₀cycloalkyl,C₃-C₁₀hetcycloalkyl, aryl, hetaryl, arylC₁-C₆alkyl,C₁-C₆alkyloxyC₁-C₆alkyl, hetarylC₁-C₆alkyl, aryl-R⁶—C₁-C₆alkyl,hetaryl-R⁶—C₁-C₆alkyl or arylC₁-C₆alkyl-R⁶—C₁-C₆alkyl wherein the alkyl,cycloalkyl, hetcycloalkyl, alkenyl, alkynyl, aryl and hetaryl groupsindependently are optionally substituted with one or more of R⁷;

R⁴ and R⁵ independently are hydrogen, hydroxy, oxo, cyano, halo,methylendioxo, NR⁸R⁹, C₁-C₈alkyl, C₁-C₆alkyloxy, trihalomethyl,trihalomethyloxy, C₃-C₁₀cycloalkyl, C₃-C₁₀hetcycloalkyl,C₃-C₁₀cycloalkenyl, aryl, hetaryl, hetarylSO_(n), arylC₁-C₆alkyloxy,hetarylC₁-C₆alkyloxy, C₁-C₆alkylR⁶—C₁-C₆alkyl,arylC₁-C₆alkyl-R⁶—C₁-C₆alkyl, C₁-C₆alkylcarbonyl, arylcarbonyl,arylC₁-C₆alkylcarbonyl, hetarylcarbonyl, hetarylC₁-C₆alkyl-carbonyl,C₁-C₆alkylSO_(n), C₁-C₆alkyl-carboxy, arylcarboxy, hetarylcarboxy,arylC₁-C₆alkylcarboxy or hetarylC₁-C₆alkylcarboxy wherein the alkyl,cycloalkyl, hetcycloalkyl, aryl and hetaryl groups independently areoptionally substituted with one or more of R¹⁵;

R⁶ is oxygen, sulphur, SO_(n), NR¹⁶;

R⁷ is hydrogen, halo, hydroxyl, cyano, nitro, COOR¹⁷, C₁-C₈alkyl,C₃-C₁₀cycloalkyl, C₃-C₁₀hetcycloalkyl, methylendioxo, trihalomethyl,trihalomethyloxy, aryl, arylC₁-C₆alkyl, C₁-C₆alkyloxy,C₁-C₆alkyloxyC₁-C₆alkyl, aryloxy, aryloxyC₁-C₆alkyl,arylC₁-C₆alkyloxyC₁-C₆alkyl, hetaryl, hetarylC₁-C₆alkyl, hetaryloxy,hetarylC₁-C₆alkyloxy, hetaryloxyC₁-C₆alkyl,hetarylC₁-C₆alkyloxyC₁-C₆alkyl, NR⁸R⁹, SO₂NR⁸R⁹, NR⁴R⁵carbonylalkyl,arylcarbonylNR⁸, arylthio, hetarylthio, arylSO_(n), hetarylSO_(n),arylSO_(m)NR⁸, arylthioC₁-C₆alkyl, hetarylthioC₁-C₆alkyl orarylC₁-C₆alkylR⁶C₁-C₆alkyl; wherein the aryl and hetaryl groupsindependently are optionally substituted with one or more R¹⁰;

R⁸ and R⁹ independently are hydrogen, C₁-C₈alkyl, aryl, hetaryl,arylC₁-C₆alkyl or hetarylC₁-C₆alkyl wherein the alkyl, aryl and hetarylgroups independently are optionally substituted with one or more of R¹¹;or

R⁸ and R⁹ together with the nitrogen to which they are attached, areforming a saturated or partially saturated cyclic, bicyclic or tricyclicring system containing from 4 to 10 carbon atoms and from 0 to 2additional heteroatoms selected from nitrogen, oxygen or sulfur, thering system optionally being substituted with at least one C₁-C₈alkyl,aryl, hetaryl, arylC₁-C₆alkyl, hetarylC₁-C₆alkyl, hydroxy, oxo,C₁-C₆alkyloxy, arylC₁-C₆alkyloxy, hetarylC₁-C₆alkyloxy,C₁-C₆alkyloxyC₁-C₆alkyl, C₁-C₆alkylcarbonyl, arylcarbonyl,hetarylcarbonyl, arylC₁-C₆alkylcarbonyl, hetarylC₁-C₆alkylcarbonyl,C₁-C₆alkylcarboxy, arylcarboxy, hetarylcarboxy, arylC₁-C₆alkyl-carboxyor hetarylC₁-C₆alkylcarboxy;

R¹⁰ and R¹¹ independently are hydrogen, hydroxy, oxo, halo, cyano,nitro, C₁-C₆alkyl, C₁-C₆-alkyloxy, NR¹²R¹³, methylendioxo, trihalomethylor trihalomethyloxy;

R¹² and R¹³ independently are hydrogen, C₁-C₈alkyl or arylC₁-C₆alkyl;

R¹⁴ is hydrogen, halo, hydroxy, oxo, nitro, cyano, C₁-C₈alkyl,C₁-C₆alkyloxy or aryloxy;

R¹⁵ is hydrogen, halo, hydroxy, oxo, nitro, cyano or COOR¹⁷;

R¹⁶ is hydrogen, C₁-C₈alkyl, C₃-C₁₀cycloalkyl, C₃-C₁₀hetcycloalkyl,aryl, arylC₁-C₆alkyl, hetaryl, hetarylC₁-C₆alkyl, alkylcarbonyl,arylcarbonyl, arylC₁-C₆alkylcarbonyl, aryloxyC₁-C₆alkyl,hetaryloxyC₁-C₆alkyl, arylthioC₁-C₆alkyl or hetarylthioC₁-C₆alkyl;wherein the alkyl, cycloalkyl, hetcycloalkyl, aryl and hetaryl groupsindependently are optionally substituted with one or more of R¹⁰;

R¹⁷ is hydrogen, C₁-C₈alkyl, aryl or arylC₁-C₆alkyl;

m is 1 or 2;

n is 0, 1 or 2; or

a salt thereof with a pharmaceutically acceptable acid or base, or anyoptical isomer or mixture of optical isomers, including a racemicmixture, or any tautomeric forms.

In another embodiment, the invention provides the present use of asubstituted amide, or a prodrug thereof of the general formula (I)wherein R¹ is C₃-C₁₀cycloalkyl or C₃-C₁₀hetcycloalkyl wherein thecycloalkyl and hetcycloalkyl groups independently are optionallysubstituted with one or more of R⁴ as defined above.

In another embodiment, the invention provides the present use of asubstituted amide, or a prodrug thereof of the general formula (I)wherein R¹ is C₃-C₁₀cycloalkyl optionally substituted with one or moreof R⁴ as defined above.

In another embodiment, the invention provides the present use of asubstituted amide, or a prodrug thereof of the general formula (I)wherein R² is hydrogen or C₁-C₈alkyl, wherein the alkyl group isoptionally substituted with one or more of R⁵ as defined above.

In another embodiment, the invention provides the present use of asubstituted amide, or a prodrug thereof of the general formula (I)wherein R² is C₁-C₈alkyl optionally substituted with one or more of R⁵as defined above.

In another embodiment, the invention provides the present use of asubstituted amide, or a prodrug thereof of the general formula (I)wherein R³ is C₃-C₁₀cycloalkyl, C₃-C₁₀hetcycloalkyl, aryl, hetaryl,arylC₁-C₆alkyl, hetarylC₁-C₆alkyl, aryl-R⁶—C₁-C₆alkyl,hetaryl-R⁶—C₁-C₆alkyl or arylC₁-C₆alkyl-R⁶—C₁-C₆alkyl wherein the alkyl,cycloalkyl, hetcycloalkyl, aryl and hetaryl groups independently areoptionally substituted with one or more of R⁷.

In another embodiment, the invention provides the present use of asubstituted amide, or a prodrug thereof of the general formula (I)wherein R³ is aryl or hetaryl, wherein the aryl and hetaryl groups areoptionally substituted with one or more of R⁷ as defined above.

In another embodiment, the invention provides the present use of asubstituted amide, or a prodrug thereof of the general formula (I)wherein R³ is phenyl optionally substituted with one or more of R⁷ asdefined above.

In another embodiment, the invention provides the present use of asubstituted amide, or a prodrug thereof of the general formula (I)wherein R³ is phenyl optionally substituted independently in position2(ortho) or 4(para) with one or more of R⁷ as defined above.

In another embodiment, the invention provides the present use of asubstituted amide, or a prodrug thereof of the general formula (I)wherein R⁴ and R⁵ independently are hydrogen, hydroxy, oxo, halo,C₁-C₈alkyl, wherein the alkyl group is optionally substituted with oneor more of R¹⁵.

In another embodiment, the invention provides the present use of asubstituted amide, or a prodrug thereof of the general formula (I)wherein R⁶ is oxygen.

In another embodiment, the invention provides the present use of asubstituted amide, or a prodrug thereof of the general formula (I)wherein R⁷ is hydrogen, halo, hydroxy, cyano, C₁-C₈alkyl,C₃-C₁₀cycloalkyl, C₃-C₁₀hetcycloalkyl, trihalomethyl, aryl,arylC₁-C₆alkyl, C₁-C₆alkyloxy, C₁-C₆alkyloxyC₁-C₆alkyl, aryloxy,arylC₁-C₆alkyloxy, aryloxyC₁-C₆alkyl, arylC₁-C₆alkyloxyC₁-C₆alkyl,hetaryl, hetarylC₁-C₆alkyl, hetaryloxy, hetarylC₁-C₆alkyloxy,hetaryloxyC₁-C₆alkyl, hetarylC₁-C₆alkyl-oxyC₁-C₆alkyl, NR⁸R⁹,NR⁴R⁵carbonylC₁-C₆alkyl, R¹⁸carbonylNR⁸, R¹⁹SO_(m)NR⁸, wherein the aryland hetaryl groups independently are optionally substituted with one ormore R¹⁰.

In another embodiment, the invention provides the present use of asubstituted amide, or a prodrug thereof of the general formula (I)wherein R⁸ and R⁹ together with the nitrogen to which they are attached,are forming a saturated or partially saturated cyclic, bicyclic ortricyclic ring system containing from 4 to 10 carbon atoms and from 0 to2 additional heteroatoms selected from nitrogen, oxygen or sulfur, thering system optionally being substituted with at least one halo, cyano,C₁-C₈alkyl, aryl, hetaryl, arylC₁-C₆alkyl, hetarylC₁-C₆alkyl, hydroxy,oxo, C₁-C₆alkyloxy, arylC₁-C₆alkyloxy, hetarylC₁-C₆alkyloxy,C₁-C₆alkyloxyC₁-C₆alkyl, C₁-C₆alkylcarbonyl, arylcarbonyl,hetarylcarbonyl, arylC₁-C₆alkylcarbonyl, hetarylC₁-C₆alkylcarbonyl,C₁-C₆alkylcarboxy, arylcarboxy, hetarylcarboxy, arylC₁-C₆alkylcarboxy orhetarylC₁-C₆alkylcarboxy.

In another embodiment, the invention provides the present use of asubstituted amide, or a prodrug thereof of the general formula (I)wherein R¹⁵ is CONR⁸R⁹.

In another embodiment, the invention provides the present use of asubstituted amide, or a prodrug thereof of the general formula (I)wherein R¹⁸ is C₁-C₆alkyl optionally substituted with R¹⁵;

-   In another embodiment, the invention provides the present use of a    substituted amide, or a prodrug thereof of general formula (I),    selected from the group consisting of:-   3-(10,11-Dihydro-dibenzo[b,f]azepin-5-yl)-1-[4-(1H-imidazol-4-yl)-piperidin-1-yl]-propan-1-one;-   4-(10,11-Dihydro-dibenzo[b,f]azepin-5-yl)-1-[4-(3H-imidazol-4-yl)-piperidin-1-yl]-butan-1-one;-   2,4-Bis-benzyloxy-benzamide;-   (1H-Indol-4-yl)-piperidin-1-yl-methanone;-   N-(1,4-Dioxo-1,4-dihydro-naphthalen-2-yl)-benzamide;-   N-(2,3-Dihydroxy-propyl)-2-(2-phenyl-adamantan-2-yl)-acetamide;-   (6-Fluoro-2-methyl-3,4-dihydro-2H-quinolin-1-yl)-phenyl-methanone;-   (2-Chloro-phenyl)-(6-fluoro-2-methyl-3,4-dihydro-2H-quinolin-1-yl)-methanone;-   3-Cyclopentyl-1-(6-fluoro-2-methyl-3,4-dihydro-2H-quinolin-1-yl)-propan-1-one;-   (3-Chloro-thieno[2,3-b]thiophen-2-yl)-thiomorpholin-4-yl-methanone;-   2-[2-(4-Chloro-phenyl)-adamantan-2-yl]-1-[4-(4-methoxy-phenyl)-piperazin-1-yl]-ethanone;-   1-(4-Benzyl-piperazin-1-yl)-2-[2-(4-chloro-phenyl)-adamantan-2-yl]-ethanone;-   2-[2-(4-Chloro-phenyl)-adamantan-2-yl]-1-(4-methyl-piperazin-1-yl)-ethanone;-   1-[4-(6-Chloro-pyridin-2-yl)-piperazin-1-yl]-2-(2-phenyl-adamantan-2-yl)-ethanone;-   4-Chloro-N-(1,7,7-trimethyl-bicyclo[2.2.1]hept-2-yl)-benzamide;-   3-Chloro-benzo[b]thiophene-2-carboxylic acid    (2-cyano-ethyl)-cyclohexyl-amide;-   2-[2-(Bicyclo[2.2.1]hept-5-en-2-ylamino)-4-oxo-4,5-dihydro-thiazol-5-yl]-N-(2-chloro-phenyl)acetamide;-   [3-(4-sec-Butyl-phenoxy)-phenyl]-piperidin-1-yl-methanone;-   3-(6-Chloro-pyridin-2-yloxy)-N-ethyl-benzamide;-   N-Benzyl-2,4-dichloro-N-pyridin-2-yl-benzamide;-   2-[Benzoyl-(3-chloro-4-fluoro-phenyl)-amino]-propionic acid butyl    ester;-   2-[Benzoyl-(3-chloro-4-fluoro-phenyl)-amino]-propionic acid pentyl    ester;-   3-(4-Fluoro-phenyl)-1-(4-phenyl-piperidin-1-yl)-but-2-en-1-one;-   N-(1,7,7-Trimethyl-bicyclo[2.2.1]hept-2-yl)-benzamide;-   1-(3-Cyclopentyl-propionyl)-piperidine-3-carboxylic acid ethyl    ester;-   4-Phenyl-1-phenylacetyl-piperidine-4-carbonitrile;-   1-Octanoyl-4-phenyl-piperidine-4-carbonitrile;-   2,2-Dimethyl-1-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-propan-1-one;-   (4-Chloro-phenyl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone;-   N-[1-(4-Methanesulfonyl-phenyl)-ethyl]-N-(tetrahydro-furan-2-ylmethyl)-benzamide;-   2-(2-Amino-phenylsulfanyl)-1-(5-fluoro-2,3-dihydro-indol-1-yl)-ethanone;-   N-(1-Methyl-2,3-dihydro-1H-indol-5-ylmethyl)-N-(tetrahydro-furan-2-ylmethyl)-benzamide;-   1-Benzoyl-piperidine-2-carboxylic acid ethyl ester;-   N-(2-Chloro-phenyl)-2-(1,2,3,4-tetrahydro-isoquinolin-1-yl)-acetamide;-   (Decahydro-naphthalen-1-yl)-(4-methyl-piperazin-1-yl)-methanone;-   (4-Methyl-piperazin-1-yl)-(2-p-tolylsulfanyl-phenyl)-methanone;-   Adamantane-1-carboxylic acid    (3-benzyloxy-2-ethyl-6-methyl-pyridin-4-yl)-amide;-   (6-Fluoro-2-methyl-3,4-dihydro-2H-quinolin-1-yl)-(3,4,5-trimethoxy-phenyl)-methanone;-   N-Bicyclo[2.2.1]hept-2-yl-3-cyclopentyl-propionamide;-   (2-Benzo[1,2,5]oxadiazol-5-yl-thiazol-4-yl)-piperidin-1-yl-methanone;-   Thiophene-2-carboxylic acid    [4-(4-fluoro-phenyl)-4-hydroxy-butyl]-isopropyl-amide;-   N-Cyclohexyl-3-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-propionamide;-   2-[(Adamantane-1-carbonyl)-amino]-3-(1H-indol-3-yl)-propionic acid    methyl ester;-   Adamantane-1-carboxylic acid    [3-(1H-benzoimidazol-2-ylsulfanyl)-5-nitro-phenyl]-amide;-   N-Benzyl-N-(1-cyclopropyl-ethyl)-4-fluoro-benzamide;-   Thiophene-2-carboxylic acid    2-[2-(2-phenyl-adamantan-2-yl)-acetylamino]-ethyl ester;-   N-(4-Acetyl-phenyl)-2-(2-phenyl-adamantan-2-yl)-acetamide;-   2-[2-(4-Chloro-phenyl)-adamantan-2-yl]-N-(2-hydroxy-ethyl)-acetamide;-   (4-Benzoyl-piperidin-1-yl)-thiophen-2-yl-methanone;-   N-(2-Benzoyl-4-methyl-phenyl)-3-phenyl-acrylamide;-   N-(2-Benzoyl-4-methyl-phenyl)-2-fluoro-benzamide;-   Adamantane-1-carboxylic acid (4-ethoxy-benzothiazol-2-yl)-amide;-   Adamantane-1-carboxylic acid    (5-benzoyl-4-phenyl-thiazol-2-yl)-amide;-   3-(2-Hydroxy-phenyl)-1,3-di-piperidin-1-yl-propan-1-one;-   N-(1-Methyl-2-phenyl-ethyl)-3-phenyl-propionamide;-   4-Oxo-4-piperidin-1-yl-butyric acid 4-tert-butyl-cyclohexyl ester;-   N-tert-Butyl-N-(4-methoxy-benzyl)-4-nitro-benzamide;-   {4-[(Adamantane-1-carbonyl)-amino]-phenoxy}-acetic acid;-   2-(4-Isobutyl-phenyl)-N-(1-phenyl-ethyl)-propionamide;-   Adamantane-1-carboxylic acid    4-[(adamantane-1-carbonyl)-amino]-2,6-dimethyl-pyridin-3-yl ester;-   2-Phenyl-1-(3-phenyl-pyrrolidin-1-yl)-ethanone;-   Adamantane-1-carboxylic acid    4-[(adamantane-1-carbonyl)-amino]-2-ethyl-6-methyl-pyridin-3-yl    ester;-   N-(1,3-Dioxo-1,3-dihydro-isoindol-2-ylmethyl)-N-(4-hydroxy-phenyl)-benzamide;-   Biphenyl-4-yl-piperidin-1-yl-methanone;-   Azepan-1-yl-(3,5-dichloro-phenyl)-methanone;-   Azepan-1-yl-biphenyl-4-yl-methanone;-   Azepan-1-yl-(4-chloro-phenyl)-methanone;-   3-Heptylcarbamoyl-bicyclo[2.2.1]hept-5-ene-2-carboxylic acid;-   Adamantan-1-yl-azepan-1-yl-methanone;-   N,N-Dibenzyl-3,4-dimethoxy-benzamide;-   N-Benzyl-N-isopropyl-4-nitro-benzamide;-   N-[2-(1H-Indol-3-yl)-1-methyl-ethyl]-2-(4-isobutyl-phenyl)-propionamide;-   N-tert-Butyl-2-(4-isobutyl-phenyl)-propionamide;-   Adamantane-1-carboxylic acid (2-acetyl-phenyl)-amide;-   N-(1,3-Dioxo-1,3-dihydro-isoindol-2-ylmethyl)-N-(4-fluoro-phenyl)-benzamide;-   (Octahydro-quinolin-1-yl)-phenyl-methanone;-   (7-Hydroxy-octahydro-quinolin-1-yl)-phenyl-methanone;-   N-(1,3-Dioxo-1,3-dihydro-isoindol-2-ylmethyl)-N-p-tolyl-benzamide;-   N,N-Dibenzyl-4-methyl-benzamide;-   (2-Chloro-phenyl)-(2-methyl-piperidin-1-yl)-methanone;-   [4-Bromo-3-(piperidine-1-sulfonyl)-phenyl]-piperidin-1-yl-methanone;-   2-Chloro-N-(3,4-dimethyl-phenyl)-benzamide;-   1-Azepan-1-yl-2-(3,3-dimethyl-3,4-dihydro-2H-isoquinolin-1-ylidene)-ethanone;-   N-Cyclohexyl-4-(2,4-dichloro-phenoxy)-butyramide;-   N-Benzo[1,3]dioxol-5-yl-2-chloro-benzamide;-   (4-Benzyl-piperidin-1-yl)-(2-chloro-phenyl)-methanone;-   2-(Benzothiazol-2-ylsulfanyl)-N-cyclohexyl-acetamide;-   Cyclohexanecarboxylic acid    (7,7-dimethyl-5-oxo-5,6,7,8-tetrahydro-quinazolin-2-yl)-amide;-   2,4-Dichloro-N-ethyl-N-o-tolyl-benzamide;-   (4-Benzyl-piperidin-1-yl)-(4-fluoro-phenyl)-methanone;-   N-Cyclohexyl-4-(2,4-dichloro-phenoxy)-N-methyl-butyramide;-   3-[2-(1,3-Dioxo-1,3-dihydro-isoindol-2-yl)-ethyl]-adamantane-1-carboxylic    acid;-   Morpholin-4-yl-(3-p-tolyl-adamantan-1-yl)-methanone;-   N-Benzyl-2,4-dichloro-N-methyl-benzamide;-   Thiophene-2-carboxylic acid dibenzylamide;-   Azepan-1-yl-(2-bromo-phenyl)-methanone;-   (3,4-Dichloro-phenyl)-(4-methyl-piperidin-1-yl)-methanone;-   N,N-Dibenzyl-3,4-dichloro-benzamide;-   4-(2,4-Dichloro-phenoxy)-1-piperidin-1-yl-butan-1-one;-   N,N-Dibenzyl-2-fluoro-benzamide;-   (2-Chloro-phenyl)-piperidin-1-yl-methanone;-   2-Chloro-N-(3-trifluoromethyl-phenyl)-benzamide;-   N-Benzyl-N-ethyl-2-phenyl-acetamide;-   (3,4-Dihydro-2H-quinolin-1-yl)-p-tolyl-methanone;-   Thiophene-2-carboxylic acid benzyl-ethyl-amide;-   N-Adamantan-1-yl-2-dibenzylamino-acetamide;-   N-Cyclohexyl-2-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-3-phenyl-propionamide;-   Thiophene-2-carboxylic acid cycloheptylamide;-   N-Cyclohexyl-3-diethylsulfamoyl-4-methyl-benzamide;-   4-Benzoyl-N-methyl-N-phenyl-benzamide;-   N-Benzyl-2-bromo-N-methyl-benzamide;-   2-Chloro-N-methyl-N-phenyl-benzamide;-   4-Chloro-N-ethyl-N-o-tolyl-benzamide;-   N-Benzyl-4,N-dimethyl-benzamide;-   2-(4-Chloro-3,5-dimethyl-phenoxy)-N-cyclohexyl-N-methyl-acetamide;-   N-Benzyl-2-bromo-N-isopropyl-benzamide;-   3-(2-Chloro-phenyl)-N-cyclohexyl-N-methyl-acrylamide;-   N-Phenyl-N-(2,2,5-trimethyl-hex-4-enyl)-acetamide;-   N-m-Tolyl-N-(2,2,5-trimethyl-hex-4-enyl)-acetamide;-   (3-Chloro-benzo[b]thiophen-2-yl)-(4-methyl-piperazin-1-yl)-methanone;-   Adamantane-1-carboxylic acid (5-methyl-pyridin-2-yl)-amide;-   3-Bromo-N-[2-methyl-1-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]octane-6-carbonyl)-butyl]-benzamide;-   4-Chloro-N-[2-methyl-1-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]octane-6-carbonyl)-butyl]-benzamide;-   4-Methyl-N-[2-methyl-1-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]octane-6-carbonyl)-butyl]benzamide;-   Cyclohexanecarboxylic acid    [2-methyl-1-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]octane-6-carbonyl)butyl]-amide;-   3-Cyclopentyl-N-[2-methyl-1-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]octane-6-carbonyl)-butyl]-propionamide;-   2-Chloro-N-[2-(4-ethyl-benzoylamino)-ethyl]-N-(4-fluoro-phenyl)-benzamide;-   N-{1-Benzyl-2-[4-(3-cyclopentyl-propionyl)-piperazin-1-yl]-2-oxo-ethyl}-3-cyclopentyl-propionamide;-   N-Bicyclo[2.2.1]hept-5-en-2-ylmethyl-3-cyclopentyl-N-[2-(1H-indol-3-yl)-ethyl]-propionamide;-   N-Bicyclo[2.2.1]hept-5-en-2-ylmethyl-2,4-dichloro-N-[2-(1H-indol-3-yl)-ethyl]-benzamide;-   Naphthalene-2-carboxylic acid    (2-oxo-azepan-3-yl)-thiophen-3-ylmethyl-amide;-   3,4,5-Trimethoxy-N-(4-methyl-benzyl)-N-[6-(pyridin-2-ylamino)-hexyl]-benzamide;-   3-Cyclopentyl-N-(4-methyl-benzyl)-N-[6-(pyridin-2-ylamino)-hexyl]-propionamide;-   N-(3,4-Dimethoxy-benzyl)-3-methoxy-N-[6-(pyridin-2-ylamino)-hexyl]-benzamide;-   N,N-Dimethyl-2-[3-(4-nitro-phenyl)-adamantan-1-yl]-acetamide;-   Adamantane-1-carboxylic acid    [4-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-butyl]-p-tolyl-amide;-   2-(1,3-Dioxo-1,3-dihydro-isoindol-2-yl)-3-methyl-N-(2-trifluoromethyl-phenyl)-butyramide;-   2-(4-Chloro-2-methyl-phenoxy)-N-(2-trifluoromethyl-phenyl)-propionamide;-   4-(2,4-Dichloro-phenoxy)-1-[4-(4-fluoro-phenyl)-piperazin-1-yl]-butan-1-one;-   (3,4-Dihydro-2H-quinolin-1-yl)-[3-(piperidine-1-sulfonyl)-phenyl]-methanone;-   Acetic acid 4-(azepane-1-carbonyl)-phenyl ester;-   N-Adamantan-1-ylmethyl-benzamide;-   [3-(4-Nitro-phenyl)-adamantan-1-yl]-piperidin-1-yl-methanone;-   N-(1,1-Dimethyl-hexyl)-2-morpholin-4-yl-acetamide;-   Adamantyl-1-carboxylic acid (2-methoxy-ethyl)-amide;-   N-(4-Adamantan-1-yl-2-methyl-phenyl)-acetamide;-   3-p-Tolyl-adamantane-1-carboxylic acid (2,5-dichloro-phenyl)-amide;-   (3-Chloro-adamantan-1-yl)-pyrrolidin-1-yl-methanone;-   2-Amino-5-cyclohexylcarbamoyl-4-methyl-thiophene-3-carboxylic acid    ethyl ester;-   N-(2-Chloro-phenyl)-2-{3-[(2-chloro-phenylcarbamoyl)-methyl]-adamantan-1-yl}-acetamide;-   3-p-Tolyl-adamantane-1-carboxylic acid (2,4-difluoro-phenyl)-amide;-   Adamantyl-1-carboxylic acid tert-butylamide;-   2-Adamantan-1-yl-N-tert-butyl-acetamide;-   N-Methyl-N-phenyl-4-(pyrrolidine-1-sulfonyl)-benzamide;-   N-(1-Adamantan-1-yl-ethyl)-2-fluoro-benzamide;-   Adamantane-1-carboxylic acid [2-(3,4-dimethoxy-phenyl)-ethyl]-amide;-   Adamantane-1-carboxylic acid dimethylamide;-   N-Benzyl-4-chloro-N-(1-cyclopropyl-vinyl)-benzamide;-   3,5-Dimethyl-adamantane-1-carboxylic acid benzylamide;-   2,4-Dichloro-N-cyclohexyl-N-(2-hydroxy-ethyl)-benzamide;-   N-Adamantan-1-yl-2,4-dichloro-N-ethyl-benzamide;-   2-[(3-p-Tolyl-adamantane-1-carbonyl)-amino]-propionic acid methyl    ester;-   N-Adamantan-1-yl-3-morpholin-4-yl-propionamide;-   3-p-Tolyl-adamantane-1-carboxylic acid isopropylamide;-   N-Adamantan-1-yl-2-benzylamino-acetamide;-   N-Benzyl-2,4-dichloro-N-(1-cyclopropyl-ethyl)-5-methyl-benzamide;-   2-[(Adamantane-1-carbonyl)-amino]-benzoic acid ethyl ester;-   N-Benzyl-N-isopropyl-4-methyl-3-nitro-benzamide;-   (3,4-Dihydro-2H-quinolin-1-yl)-(2-fluoro-phenyl)-methanone;-   N-Ethyl-2-fluoro-N-phenyl-benzamide;-   2-Phenethyl-N-(2-trifluoromethyl-phenyl)-benzamide;-   1-(3,4-Dihydro-2H-quinolin-1-yl)-2-o-tolyloxy-ethanone;-   2-(1-Benzyl-1H-imidazol-2-ylsulfanyl)-N-cyclohexyl-acetamide;-   Cyclohexanecarboxylic acid (2-propoxy-phenyl)-amide;-   2-{3-[4-(2-Chloro-phenyl)-piperazin-1-yl]-3-oxo-propyl}-isoindole-1,3-dione;-   N-Cyclopentyl-2-(2,4-dichloro-phenoxy)-propionamide;-   Adamantane-1-carboxylic acid (2-trifluoromethyl-phenyl)-amide;-   (4-Chloro-3-nitro-phenyl)-(2,6-dimethyl-piperidin-1-yl)-methanone;-   4-(2-Ethyl-phenyl)-4-aza-tricyclo[5.2.2.0^(2,6)]undec-8-ene-3,5-dione;-   2-Phenyl-N-(2-trifluoromethyl-phenyl)-butyramide;-   N-Adamantan-1-yl-4-chloro-2-nitro-benzamide;-   3-p-Tolyl-adamantane-1-carboxylic acid (2,3-dimethyl-phenyl)-amide;-   N-Benzyl-3-methyl-4-p-tolyl-butyramide;-   N-(2-Cyclohex-1-enyl-ethyl)-2-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-propionamide;-   (4-tert-Butyl-phenyl)-(3,4-dihydro-1H-isoquinolin-2-yl)-methanone;-   2-[1-(4-Chloro-benzenesulfonyl)-1H-benzoimidazol-2-ylsulfanyl]-N-thiophen-2-ylmethyl-acetamide;-   2-Phenoxy-1-[4-(2-trifluoromethyl-benzyl)-piperazin-1-yl]-ethanone;-   Cyclohexanecarboxylic acid    [5-(2-fluoro-benzylsulfanylmethyl)-[1,3,4]thiadiazol-2-yl]-amide;-   4-Methyl-2-phenyl-thiazole-5-carboxylic acid naphthalen-1-ylamide;-   4-Fluoro-N-[4-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]octane-6-carbonyl)-phenyl]-benzenesulfonamide;-   (3-Methoxy-phenyl)-(4-o-tolyl-piperazin-1-yl)-methanone;-   N-Adamantan-1-yl-3-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-propionamide;-   N-Cyclooctyl-2-methoxy-3-methyl-benzamide;-   2-[4-(2,3,3-Trimethyl-6-aza-bicyclo[3.2.1]octane-6-carbonyl)-phenyl]-isoindole-1,3-dione;-   (2,3-Diphenyl-quinoxalin-6-yl)-(2,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone;-   Adamantan-1-yl-(1,3,4,5-tetrahydro-pyrido[4,3-b]indol-2-yl)-methanone;-   N-{4-[1-(Naphthalene-2-sulfonyl)-piperidin-3-yl]-butyl}-N′-p-tolyl-oxalamide;-   N-Benzyl-N-(2-oxo-2-pyrrolidin-1-yl-ethyl)-benzenesulfonamide;-   (4-Amino-phenyl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone;-   1-[4-(4-Fluoro-phenyl)-piperazin-1-yl]-2-(2-isopropyl-5-methyl-phenoxy)-ethanone;-   Adamantane-1-carboxylic acid benzyl-pyridin-2-yl-amide;-   Adamantan-1-yl-piperidin-1-yl-methanone;-   Adamantan-1-yl-pyrrolidin-1-yl-methanone;-   (3,4-Dihydro-2H-quinolin-1-yl)-o-tolyl-methanone;-   Adamantyl-1-carboxylic acid benzylamide;-   Pyridine-2-carboxylic acid adamantan-2-ylamide;-   (3-Chloro-adamantan-1-yl)-piperidin-1-yl-methanone;-   Adamantan-1-yl-(4-methyl-piperidin-1-yl)-methanone;-   2-[3-(Azepane-1-carbonyl)-phenyl]-isoindole-1,3-dione;-   2-[3-(Piperidine-1-carbonyl)-phenyl]-isoindole-1,3-dione;-   4-(Benzyl-methanesulfonyl-amino)-N-furan-2-ylmethyl-benzamide;-   (4-Nitro-phenyl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone;-   1-Cyclohexyl-5-oxo-pyrrolidine-3-carboxylic acid    (4-chloro-3-nitro-phenyl)-amide;-   N-(2-Chloro-phenyl)-2-(2-oxo-2-phenyl-ethylsulfanyl)-acetamide;-   3-(4-Hydroxy-phenyl)-N-isochroman-1-ylmethyl-3-phenyl-propionamide;-   (4-Ethoxy-phenyl)-(2-methyl-piperidin-1-yl)-methanone;-   1-Cyclohexyl-5-oxo-pyrrolidine-3-carboxylic acid    (3-chloro-phenyl)-amide;-   N-[4-(Benzyl-isopropyl-sulfamoyl)-phenyl]-acetamide;-   N-(3,4-Dimethyl-phenyl)-N-[4-(piperidine-1-carbonyl)-benzyl]-methanesulfonamide;-   2-(5-Phenyl-1H-imidazol-2-ylsulfanyl)-N-(1,1,3,3-tetramethyl-butyl)-acetamide;-   2-(Benzothiazol-2-ylsulfanyl)-N-(1,1,3,3-tetramethyl-butyl)-acetamide;-   2-(Benzooxazol-2-ylsulfanyl)-N-(1,1,3,3-tetramethyl-butyl)-acetamide;-   2-(Naphthalen-2-ylcarbamoylmethylsulfanyl)-N-(1,1,3,3-tetramethyl-butyl)-acetamide;-   Acetic acid 4-(3,5-dimethyl-piperidine-1-carbonyl)-phenyl ester;-   [1-(4-Chloro-benzenesulfonyl)-piperidin-3-yl]-(octahydro-quinolin-1-yl)-methanone;-   (4-Fluoro-phenyl)-(3,4,4a,8a-tetrahydro-2H-quinolin-1-yl)-methanone;-   N-Adamantan-1-yl-2-ethoxy-acetamide;-   2-(2-Oxo-2-phenothiazin-10-yl-ethyl)-hexahydro-isoindole-1,3-dione;-   Adamantane-1-carboxylic acid (tetrahydro-furan-2-ylmethyl)-amide;-   2-Bromo-N-cycloheptyl-benzamide;-   Bicyclo[2.2.1]hept-2-yl-[4-(2-ethoxy-phenyl)-piperazin-1-yl]-methanone;-   N-Furan-2-ylmethyl-2-phenyl-2-phenylsulfanyl-acetamide;-   Adamantane-1-carboxylic acid benzyl-methyl-amide;-   1-(3,4-Dihydro-2H-quinolin-1-yl)-3-(4-fluoro-phenyl)-propenone;-   Adamantan-1-yl-(2,6-dimethyl-piperidin-1-yl)-methanone;-   4-Methyl-N-homoadamantyl-3-yl-benzamide;-   (3,5-Dimethyl-piperidin-1-yl)-(3-methyl-4-nitro-phenyl)-methanone;-   Quinoline-2-carboxylic acid cyclooctylamide;-   Adamantane-1-carboxylic acid [2-(2,4-dimethoxy-phenyl)-ethyl]-amide;-   (3,4-Dihydro-1H-isoquinolin-2-yl)-o-tolyl-methanone;-   (3,6-Dichloro-benzo[b]thiophen-2-yl)-(4-methyl-piperazin-1-yl)-methanone;-   3-(1-Benzyl-1H-imidazol-2-ylsulfanyl)-N-cyclohexyl-propionamide;-   Propionic acid 2-amino-4-methyl-5-p-tolylcarbamoyl-thiophen-3-yl    ester;-   2-Cyclohexyl-N-(2,6-dimethyl-phenyl)-N-furan-2-ylmethyl-acetamide;-   (3-Methoxy-phenyl)-(2,2,4-trimethyl-4-phenyl-3,4-dihydro-2H-quinolin-1-yl)-methanone;-   1-[4-(2,3,3-Trimethyl-6-aza-bicyclo[3.2.1]octane-6-carbonyl)-phenyl]-pyrrolidine-2,5-dione;-   1-(3,4-Dihydro-2H-quinolin-1-yl)-2-(1-naphthalen-1-yl-1H-tetrazol-5-ylsulfanyl)-ethanone;-   [4-(2,3-Dimethyl-phenyl)-piperazin-1-yl]-o-tolyl-methanone;-   (4-Benzyl-piperidin-1-yl)-(4-methyl-3-nitro-phenyl)-methanone;-   N-(2-Cyano-phenyl)-2-(9-ethyl-9H-1,3,4,9-tetraaza-fluoren-2-ylsulfanyl)-acetamide;-   N-(2-Cyano-phenyl)-2-(9-methyl-9H-1,3,4,9-tetraaza-fluoren-2-ylsulfanyl)-acetamide;-   1-(Thiophene-2-carbonyl)-2,3-dihydro-1H-quinolin-4-one;-   (3-Chloro-6-nitro-benzo[b]thiophen-2-yl)-piperidin-1-yl-methanone;-   (4-Bromo-phenyl)-(3,5-dimethyl-piperidin-1-yl)-methanone;-   2-Morpholin-4-yl-N-(1-phenyl-cyclopentylmethyl)-acetamide;-   9-Oxo-9H-fluorene-1-carboxylic acid (3-methyl-butyl)-amide;-   [4-(2,5-Dimethyl-pyrrol-1-yl)-phenyl]-(4-methyl-piperidin-1-yl)-methanone;-   N-Cycloheptyl-3-diethylsulfamoyl-benzamide;-   (4-Methoxy-phenyl)-(3-phenyl-piperidin-1-yl)-methanone;-   3-Amino-N-cyclohexyl-N-methyl-benzamide;-   N-Ethyl-3,4-dimethyl-N-phenyl-benzamide;-   N-Benzyl-3,4,N-trimethyl-benzamide;-   (4-Fluoro-phenyl)-(3-phenyl-piperidin-1-yl)-methanone;-   [4-(2,3-Dimethyl-phenyl)-piperazin-1-yl]-(3-methoxy-phenyl)-methanone;-   Furan-2-carboxylic acid    [4-(4-methyl-piperidine-1-sulfonyl)-phenyl]-amide;-   N-(2-Cyclohex-1-enyl-ethyl)-2-o-tolyloxy-acetamide;-   5-(2-Chloro-phenoxymethyl)-furan-2-carboxylic acid    (1-bicyclo[2.2.1]hept-2-yl-ethyl)-amide;-   3-(2-Chloro-phenyl)-1-[4-(2,3-dimethyl-phenyl)-piperazin-1-yl]-propenone;-   N-[3-(Azepane-1-carbonyl)-phenyl]-benzamide;-   [3-(Piperidine-1-carbonyl)-pyrazol-1-yl]-o-tolyl-methanone;-   N-(1-Phenyl-cyclopentylmethyl)-2-piperidin-1-yl-propionamide;-   2-Morpholin-4-yl-N-(1-phenyl-cyclopentylmethyl)-propionamide;-   N-[4-(Azepane-1-sulfonyl)-phenyl]-2,2,2-trifluoro-acetamide;-   2,3-Dihydro-benzo[1,4]dioxine-6-carboxylic acid    (1-adamantan-1-yl-ethyl)-amide;-   N-Adamantan-1-yl-2-(3-methoxy-phenoxy)-acetamide;-   3-Chloro-benzo[b]thiophene-2-carboxylic acid    (2-cyano-ethyl)-phenyl-amide;-   [4-(4-Nitro-benzyl)-piperidin-1-yl]-phenyl-methanone;-   [4-(2-Nitro-benzyl)-piperidin-1-yl]-phenyl-methanone;-   3-[5-(4-Fluoro-phenyl)-furan-2-yl]-1-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-propenone;-   2-(3-Fluoro-benzoylamino)-4-methyl-5-(piperidine-1-carbonyl)-thiophene-3-carboxylic    acid methyl ester;-   N-(2-Ethyl-phenyl)-2-(3-methyl-piperidin-1-yl)-acetamide;-   2-(2-Methoxy-benzoylamino)-4-methyl-5-(piperidine-1-carbonyl)-thiophene-3-carboxylic    acid methyl ester;-   1-Phenyl-cyclopentanecarboxylic acid    (4-phenyl-tetrahydro-pyran-4-ylmethyl)-amide;-   4-(2,4-Dichloro-phenoxy)-1-(4-phenyl-piperazin-1-yl)-butan-1-one;-   Naphthalene-1-carboxylic acid cycloheptylamide;-   N-Indan-5-yl-2-methyl-3-nitro-benzamide;-   N-Cyclohexyl-3-(2,2,2-trifluoro-ethoxymethyl)-benzamide;-   2-Methoxy-N-(1-phenyl-cyclopentylmethyl)-benzamide;-   [5-(2,5-Dichloro-phenoxymethyl)-furan-2-yl]-(2,6-dimethyl-morpholin-4-yl)-methanone;-   [5-(2-Bromo-phenoxymethyl)-furan-2-yl]-(2-methyl-piperidin-1-yl)-methanone;-   5-(2-Methoxy-phenoxymethyl)-furan-2-carboxylic acid    cycloheptylamide;-   (3,4-Dihydro-1H-isoquinolin-2-yl)-[1-(2-nitro-benzenesulfonyl)-piperidin-3-yl]-methanone;-   N-Cyclooctyl-2-(4-methoxy-phenoxy)-acetamide;-   N-(2,3-Dimethyl-phenyl)-4-[methyl-(toluene-4-sulfonyl)-amino]-butyramide;-   N-Phenyl-N-[4-(piperidine-1-carbonyl)-benzyl]-benzenesulfonamide;-   N-[4-(3,4-Dihydro-1H-isoquinoline-2-carbonyl)-benzyl]-N-(3,4-dimethyl-phenyl)methanesulfonamide;-   2,3-Dihydro-benzo[1,4]dioxine-2-carboxylic acid    bicyclo[2.2.1]hept-2-ylamide;-   4,5,6,7-Tetrahydro-benzo[b]thiophene-3-carboxylic acid    cycloheptylamide;-   N-(2-Azepan-1-yl-2-oxo-ethyl)-N-benzyl-4-fluoro-benzenesulfonamide;-   1-(2,6-Dimethyl-morpholin-4-yl)-3,3-diphenyl-propan-1-one;-   N-Bicyclo[2.2.1]hept-2-yl-4-morpholin-4-ylmethyl-benzamide;-   [3-(2-Chloro-6-nitro-phenoxy)-phenyl]-piperidin-1-yl-methanone;-   N-Adamantan-1-yl-2-(4-methyl-quinolin-2-ylsulfanyl)-acetamide;    Cyclohexanecarboxylic acid (2-phenylsulfanyl-phenyl)-amide;-   (4-Hydroxy-4-phenyl-octahydro-quinolin-1-yl)-phenyl-methanone;-   3-Cyclohexyl-N-(3-phenyl-propyl)-propionamide;-   2-[1-(2,5-Dimethyl-phenyl)-1H-tetrazol-5-ylsulfanyl]-N-isopropyl-N-phenyl-acetamide;-   N-{2-[4-(3,4-Dihydro-1H-isoquinoline-2-sulfonyl)-phenyl]-ethyl}-acetamide;-   N-Benzyl-N-[2-oxo-2-(4-phenyl-piperazin-1-yl)-ethyl]-benzenesulfonamide;-   [4-(2-Chloro-6-nitro-phenoxy)-phenyl]-piperidin-1-yl-methanone;-   N-Cycloheptyl-3-phenyl-propionamide;-   (3-Chloro-6-methyl-benzo[b]thiophen-2-yl)-piperidin-1-yl-methanone;-   N-Cycloheptyl-2,4-dimethoxy-benzamide;-   N-(3-Chloro-phenyl)-2-(8,11,11-trimethyl-3,4,6-triaza-tricyclo[6.2.1.0^(2,7)]undeca-2(7),3,5-trien-5-ylsulfanyl)-acetamide;-   N-(2-Nitro-phenyl)-2-(8,11,11-trimethyl-3,4,6-triaza-tricyclo[6.2.1.0^(2,7)]undeca-2(7),3,5-trien-5-ylsulfanyl)-acetamide;-   N-Phenyl-2-(8,11,11-trimethyl-3,4,6-triaza-tricyclo[6.2.1.0^(2,7)]undeca-2(7),3,5-trien-5-ylsulfanyl)acetamide;-   N-Ethyl-3-methyl-N-o-tolyl-benzamide;-   N-[5-(2,4-Dichloro-benzylsulfanyl)-[1,3,4]thiadiazol-2-yl]-2,2-dimethyl-propionamide;-   4-Bromo-1-ethyl-1H-pyrazole-3-carboxylic acid    (2-methylsulfanyl-phenyl)-amide;-   5-Benzoyl-furan-2-carboxylic acid diisopropylamide;-   N-{2-[2-(4-Bromo-phenyl)-2-oxo-ethylsulfanyl]-benzothiazol-6-yl}-acetamide;-   2-(6-Amino-benzothiazol-2-ylsulfanyl)-N-cyclohexyl-acetamide;-   N-(2-Cyclohexylcarbamoylmethylsulfanyl-benzothiazol-6-yl)-2-methoxy-benzamide;-   Benzofuran-2-yl-(4-phenyl-piperidin-1-yl)-methanone;-   1-(2-Nitro-phenyl)-piperidine-3-carboxylic acid diethylamide;-   1-(4-Nitro-phenyl)-piperidine-3-carboxylic acid diethylamide;-   5-Bromo-furan-2-carboxylic acid adamantan-2-ylamide;-   3,3-Dimethyl-pentanedioic acid bis-[(2,4-difluoro-phenyl)-amide];-   2-(3-Bromo-benzylsulfanyl)-1-(4-phenyl-piperazin-1-yl)-ethanone;-   N-(2-Azepan-1-yl-2-oxo-ethyl)-N-benzyl-4-bromo-benzenesulfonamide;-   1-(2,3-Dihydro-indol-1-yl)-2-p-tolylsulfanyl-ethanone;-   [4-(4-Bromo-benzenesulfonyl)-piperazin-1-yl]-furan-2-yl-methanone;-   [5-(2-Bromo-phenoxymethyl)-furan-2-yl]-(2,6-dimethyl-morpholin-4-yl)-methanone;-   5-(2-Chloro-phenoxymethyl)-furan-2-carboxylic acid diethylamide;-   5-(2-Bromo-phenoxymethyl)-furan-2-carboxylic acid diethylamide;-   5-(2-Chloro-phenoxymethyl)-furan-2-carboxylic acid    methyl-phenyl-amide;-   [5-(2-Chloro-phenoxymethyl)-furan-2-yl]-(4-methyl-piperidin-1-yl)-methanone;-   [3-(2,5-Dichloro-phenoxymethyl)-phenyl]-pyrrolidin-1-yl-methanone;-   [5-(4-Ethoxy-phenoxymethyl)-furan-2-yl]-(4-methyl-piperidin-1-yl)-methanone;-   3-(1,3-Dioxo-1,3-dihydro-isoindol-2-yl)-N-(2-methyl-cyclohexyl)-propionamide;-   3-(3,4-Dihydro-2H-quinoline-1-carbonyl)-N-phenyl-benzenesulfonamide;-   [3-(2,3-Dihydro-indole-1-sulfonyl)-phenyl]-(3,4-dihydro-2H-quinolin-1-yl)-methanone;-   [3-(2,5-Dimethyl-pyrrol-1-yl)-phenyl]-(4-methyl-piperidin-1-yl)-methanone;-   N-Cyclohexyl-3-(2-hydroxy-4-methyl-phenyl)-3-phenyl-propionamide;-   2-Diethylamino-N-(1-phenyl-cyclopentylmethyl)-propionamide;-   (6-Fluoro-2-methyl-3,4-dihydro-2H-quinolin-1-yl)-(3-trifluoromethyl-phenyl)-methanone;-   (2,6-Dimethyl-morpholin-4-yl)-[4-(naphthalen-1-yloxymethyl)-phenyl]-methanone;-   N-Benzyl-4-bromo-N-ethyl-benzamide;-   (3-Methyl-piperidin-1-yl)-[4-(naphthalen-1-yloxymethyl)-phenyl]-methanone;-   Azepan-1-yl-[5-(2-chloro-phenoxymethyl)-furan-2-yl]-methanone;-   (4-Methyl-piperidin-1-yl)-[4-(naphthalen-1-yloxymethyl)-phenyl]-methanone;-   Azepan-1-yl-[5-(2,4-dichloro-phenoxymethyl)-furan-2-yl]-methanone;-   N-Cycloheptyl-4-(4-methoxy-2-methyl-phenyl)-butyramide;-   2-(4-Benzothiazol-2-yl-piperazin-1-yl)-N-cyclohexyl-acetamide;-   N-Cycloheptyl-2-(2,6-dimethyl-phenoxy)-acetamide;-   (3,4-Dihydro-2H-quinolin-1-yl)-(3-iodo-phenyl)-methanone;-   N-Cycloheptyl-3-(2,2,2-trifluoro-ethoxymethyl)-benzamide;-   Azepan-1-yl-[4-(2-chloro-phenoxymethyl)-phenyl]-methanone;-   (2,6-Dimethyl-morpholin-4-yl)-[4-(naphthalen-2-yloxymethyl)-phenyl]-methanone;-   Azepan-1-yl-[3-(4-ethoxy-phenoxymethyl)-phenyl]-methanone;-   Benzo[b]thiophene-3-carboxylic acid    (1,2,3,4-tetrahydro-naphthalen-1-yl)-amide;-   2-(4-Chloro-2-methyl-phenoxy)-N-cycloheptyl-acetamide;-   2,4-Dichloro-N-cyclohexyl-N-methyl-benzamide;-   N-Cyclooctyl-2-p-tolyloxy-acetamide;-   (3,5-Dimethyl-piperidin-1-yl)-(4-methyl-3-nitro-phenyl)-methanone;-   Biphenyl-4-yl-(2,6-dimethyl-piperidin-1-yl)-methanone;-   N-Cyclohexyl-4-fluoro-N-methyl-benzamide;-   N-[4-(Azepane-1-carbonyl)-phenyl]-N-methyl-benzenesulfonamide;-   N-Cycloheptyl-2-fluoro-benzamide;-   N-Cycloheptyl-4-methyl-benzamide;-   (3-Methyl-piperidin-1-yl)-p-tolyl-methanone;-   [2-(3,4-Dimethoxy-phenylcarbamoyl)-piperidin-1-yl]-acetic acid    benzyl ester;-   N-[4-(2-Methyl-piperidine-1-sulfonyl)-phenyl]-acetamide;-   2-(2,4-Dichloro-phenoxy)-N-(2-methyl-butyl)-propionamide;-   [4-(2-Chloro-6-nitro-phenyl)-piperazin-1-yl]-(4-methoxy-phenyl)-methanone;-   N-Cyclohexyl-4-(4-methoxy-3-methyl-phenyl)-butyramide;-   (3-Chloro-6-methoxy-benzo[b]thiophen-2-yl)-(3,4-dihydro-1H-isoquinolin-2-yl)-methanone;-   2-(4-Methyl-benzylsulfanyl)-1-piperidin-1-yl-ethanone;-   N-Cyclohexyl-N-[(4-phenyl-thiazol-2-ylcarbamoyl)-methyl]-benzamide;-   N-(2-Azepan-1-yl-2-oxo-ethyl)-N-(4-isopropyl-phenyl)-methanesulfonamide;-   N-Adamantan-1-yl-3-p-tolylsulfanyl-propionamide;-   6-(2,4-Dichloro-phenylcarbamoyl)-3,4-dimethyl-cyclohex-3-enecarboxylic    acid;-   (4-Butyl-cyclohexyl)-morpholin-4-yl-methanone;-   (3,4-Dichloro-phenyl)-(3,4-dihydro-2H-quinolin-1-yl)-methanone;-   N-(2-Cyclo hex-1-enyl-ethyl)-3-methoxy-benzamide;-   N-Adamantan-2-yl-3-(1,5-dimethyl-1H-pyrazol-4-yl)-acrylamide;-   N-Adamantan-1-yl-N-methyl-4-(4-nitro-pyrazol-1-ylmethyl)-benzamide;-   5-(4-Chloro-3,5-dimethyl-pyrazol-1-ylmethyl)-furan-2-carboxylic acid    adamantan-2-ylamide;-   2-(4-Chloro-phenoxy)-N-(2-fluoro-5-methyl-phenyl)-2-methyl-propionamide;-   N-Adamantan-1-yl-2-(4-chloro-3,5-dimethyl-phenoxy)-acetamide;-   2-[(3-Carboxy-bicyclo[2.2.1]heptane-2-carbonyl)-amino]-5,6-dihydro-4H-cyclopenta[b]thiophene-3-carboxylic    acid propyl ester;-   2-Adamantan-1-yl-N-[1-(2,5-dimethyl-phenyl)-ethyl]-acetamide;-   3-Methyl-thiophene-2-carboxylic acid cyclooctylamide;-   N-p-Tolyl-2-(8,11,11-trimethyl-3,4,6-triaza-tricyclo[6.2.1.0^(2,7)]undeca-2,4,6-trien-5-ylsulfanyl)propionamide;-   Azepan-1-yl-[5-(4-chloro-5-methyl-3-nitro-pyrazol-1-ylmethyl)-furan-2-yl]-methanone;-   N-Adamantan-2-yl-3-(4-bromo-3-nitro-pyrazol-1-ylmethyl)-benzamide;-   N-Bicyclo[2.2.1]hept-2-yl-2-chloro-benzamide;-   [5-(3-Chloro-phenoxymethyl)-furan-2-yl]-piperidin-1-yl-methanone;-   1-(4-Ethyl-benzoyl)-6-methoxy-2-methyl-2,3-dihydro-1H-quinolin-4-one;-   6-Fluoro-2-methyl-1-{3-[4-(propane-1-sulfonyl)-phenoxymethyl]-benzoyl}-2,3-dihydro-1H-quinolin-4-one;-   N-Cycloheptyl-2-(naphthalen-1-yloxy)-acetamide;-   N-Cyclohexyl-4-o-tolyloxy-butyramide;-   (2-Benzylsulfanyl-phenyl)-morpholin-4-yl-methanone;-   (2-Chloro-5,6-difluoro-3-methyl-phenyl)-(4-methyl-piperidin-1-yl)-methanone;-   (3-Bromo-phenyl)-[4-(4-chloro-2-nitro-phenyl)-piperazin-1-yl]-methanone;-   2-Bromo-N-(1,1,3,3-tetramethyl-butyl)-benzamide;-   N-Adamantan-1-yl-2-(2-benzoyl-5-methoxy-phenoxy)-acetamide;-   N-Cyclohexyl-3-methyl-4-p-tolyl-butyramide;-   [5-(4-Methyl-2-nitro-phenoxymethyl)-furan-2-yl]-thiomorpholin-4-yl-methanone;-   [5-(2,5-Dichloro-phenoxymethyl)-furan-2-yl]-thiomorpholin-4-yl-methanone;-   5-(4-Chloro-2-nitro-phenoxymethyl)-furan-2-carboxylic acid    adamantan-1-ylamide;-   4,5,6,7-Tetrahydro-benzo[b]thiophene-3-carboxylic acid    cyclohexylamide;-   4-Chloro-1,5-dimethyl-1H-pyrazole-3-carboxylic acid    adamantan-1-yl-methyl-amide;-   4-(4-Methoxy-3-methyl-phenyl)-N-(2-methyl-cyclohexyl)-butyramide;-   3-Benzo[1,3]dioxol-5-yl-1-(3,4-dihydro-1H-isoquinolin-2-yl)-propenone;-   N-Bicyclo[2.2.1]hept-2-yl-3-phenylsulfanyl-propionamide;-   Azepan-1-yl-[5-(2-nitro-phenoxymethyl)-furan-2-yl]-methanone;-   N-Benzyl-2-(4-chloro-phenylsulfanyl)-N-methyl-acetamide;-   1-(4-Benzyl-piperidin-1-yl)-2-benzylsulfanyl-ethanone;-   2-(4-tert-Butyl-phenoxy)-1-(4-ethyl-piperazin-1-yl)-ethanone;-   [4-(4-Ethoxy-phenoxymethyl)-phenyl]-(4-methyl-piperidin-1-yl)-methanone;-   5-(4-Bromo-3,5-dimethyl-pyrazol-1-ylmethyl)-furan-2-carboxylic acid    adamantan-2-ylamide;-   1-Azepan-1-yl-3-(4-chloro-phenylsulfanyl)-propan-1-one;-   N-Bicyclo[2.2.1]hept-2-yl-2-(2-chloro-benzylsulfanyl)-acetamide;-   2-(2-Methyl-benzylsulfanyl)-1-(4-phenyl-piperazin-1-yl)-ethanone;-   N-[2-(1-Benzo[1,3]dioxol-5-yl-3-furan-2-yl-3-oxo-propylsulfanyl)-phenyl]-acetamide;-   (3,5-Dimethyl-piperidin-1-yl)-(3-iodo-phenyl)-methanone;-   [5-(2-Bromo-phenoxymethyl)-furan-2-yl]-(6-fluoro-2-methyl-3,4-dihydro-2H-quinolin-1-yl)-methanone;-   N-Benzyl-N-cyclohex-1-enyl-isonicotinamide;-   1-[4-(4-Fluoro-phenyl)-piperazin-1-yl]-2-(2-methyl-benzylsulfanyl)-ethanone;-   2-(2-Bromo-4-methyl-phenoxy)-N-(2-cyclohex-1-enyl-ethyl)-acetamide;-   2-[5-(2-Hydroxy-phenyl)-[1,3,4]oxadiazol-2-ylsulfanyl]-1-piperidin-1-yl-ethanone;-   5-(4-Nitro-pyrazol-1-ylmethyl)-furan-2-carboxylic acid    adamantan-2-ylamide;-   3-Benzo[1,3]dioxol-5-yl-3-(2-methoxy-phenyl)-1-pyrrolidin-1-yl-propan-1-one;-   N-Adamantan-2-yl-3,4-dichloro-benzamide;-   Benzo[b]thiophen-3-yl-(6-fluoro-2-methyl-3,4-dihydro-2H-quinolin-1-yl)-methanone;-   2-Adamantan-1-yl-1-(3,4-dihydro-1H-isoquinolin-2-yl)-ethanone;-   4,5,6,7-Tetrahydro-benzo[b]thiophene-3-carboxylic acid    (2-cyclohex-1-enyl-ethyl)-amide;-   Benzo[b]thiophene-3-carboxylic acid    (3,3,5-trimethyl-cyclohexyl)-amide;-   2-(2,6-Dimethyl-phenoxy)-N-(2-isopropyl-phenyl)-acetamide;-   4-Bromo-N-[3-(piperidine-1-carbonyl)-phenyl]-benzamide;-   N-Benzo[1,3]dioxol-5-ylmethyl-2-(2-cyano-phenylsulfanyl)-benzamide;-   N-Adamantan-1-yl-2-(naphthalen-2-yloxy)-acetamide;-   [4-(4-Chloro-phenylsulfanylmethyl)-phenyl]-morpholin-4-yl-methanone;-   Thiophene-2-carboxylic acid (3,3,5-trimethyl-cyclohexyl)-amide;-   Benzo[1,3]dioxol-5-yl-(3,4-dihydro-2H-quinolin-1-yl)-methanone;-   3-Chloro-benzo[b]thiophene-2-carboxylic acid cyclooctylamide;-   2-[2-Morpholin-4-yl-1-(4-nitro-benzyl)-2-oxo-ethyl]-isoindole-1,3-dione;-   2-Hydroxy-4,4-dimethyl-6-oxo-cyclohex-1-enecarboxylic acid    phenylamide;-   (2,4-Dichloro-phenyl)-(2,6-dimethyl-piperidin-1-yl)-methanone;-   Adamantane-1-carboxylic acid furan-2-ylmethyl-p-tolyl-amide;-   Azocan-1-yl-(4-tert-butyl-phenyl)-methanone;-   3-Chloro-benzo[b]thiophene-2-carboxylic acid benzyl-methyl-amide;-   Adamantane-1-carboxylic acid (2-fluoro-phenyl)-amide;-   2-(Piperidine-1-carbonyl)-5-piperidin-1-yl-oxazole-4-carbonitrile;-   N-(4,6-Dimethyl-5-nitro-pyridin-3-yl)-benzamide;-   Adamantan-1-yl-[4-(2-methoxy-phenyl)-piperazin-1-yl]-methanone;-   (2-Methyl-piperidin-1-yl)-o-tolyl-methanone;-   N-Benzyl-4-chloro-N-isopropyl-3-nitro-benzamide;-   N-(3-Hexylsulfanyl-[1,2,4]thiadiazol-5-yl)-3-methyl-butyramide;-   4,    N-Dimethyl-N-[4-(piperidine-1-carbonyl)-phenyl]-benzenesulfonamide;-   Azepan-1-yl-(5-tert-butyl-2H-pyrazol-3-yl)-methanone;-   2-Amino-4-methyl-5-(piperidine-1-carbonyl)-thiophene-3-carboxylic    acid ethyl ester;-   5-Methyl-furan-2-carboxylic acid (1-adamantan-1-yl-ethyl)-amide;-   (3-Chloro-6-methyl-benzo[b]thiophen-2-yl)-(3,4-dihydro-1H-isoquinolin-2-yl)-methanone;-   N-Adamantan-1-yl-2-trifluoromethyl-benzamide;-   (3-Bromo-phenyl)-(2,2,4-trimethyl-4-phenyl-3,4-dihydro-2H-quinolin-1-yl)-methanone;-   Benzo[1,3]dioxole-5-carboxylic acid dipropylamide;-   N-(3,3-Diphenyl-propyl)-4-methoxy-benzamide;-   [4-(2-Chloro-6-nitro-phenyl)-piperazin-1-yl]-p-tolyl-methanone;-   Furan-2-yl-[4-(toluene-4-sulfonyl)-piperazin-1-yl]-methanone;-   3-(2-Chloro-6-fluoro-phenyl)-1-(3,4-dihydro-2H-quinolin-1-yl)-propenone;-   2-Chloro-N-cycloheptyl-benzamide;-   1-[4-(4-Nitro-phenyl)-piperazin-1-yl]-3-phenyl-propan-1-one;-   (3,4-Dihydro-1H-isoquinolin-2-yl)-(3,4-dimethyl-phenyl)-methanone;-   (1-Adamantan-1-yl-4-bromo-1H-pyrazol-3-yl)-morpholin-4-yl-methanone;-   2-Phenyl-cyclopropanecarboxylic acid cyclooctylamide;-   3-[4-(2-Ethoxy-phenyl)-piperazine-1-carbonyl]-isochromen-1-one;-   [3-(4-Bromo-pyrazol-1-ylmethyl)-phenyl]-(4-methyl-piperidin-1-yl)-methanone;-   2-Azepan-1-yl-N-biphenyl-2-yl-acetamide;-   N-[5-(3,4-Dimethoxy-benzyl)-[1,3,4]thiadiazol-2-yl]-3-methyl-butyramide;-   Adamantan-1-yl-(4-phenyl-piperidin-1-yl)-methanone;-   N-(2-Azepan-1-yl-2-oxo-ethyl)-N-(4-ethoxy-phenyl)-4-methylsulfanyl-benzenesulfonamide;-   1-Adamantan-1-yl-4-bromo-1H-pyrazole-3-carboxylic acid diethylamide;-   (6-Fluoro-2-methyl-3,4-dihydro-2H-quinolin-1-yl)-(2-fluoro-phenyl)-methanone;-   3-[4-(2,3-Dimethyl-phenyl)-piperazine-1-carbonyl]-isochromen-1-one;-   N-Cyclooctyl-2-(2-methoxy-phenoxy)-acetamide;-   N-Cyclohexyl-N-methyl-2-nitro-benzamide;-   Adamantane-1-carboxylic acid    (1,1-dioxo-tetrahydro-thiophen-3-yl)-amide;-   N-Adamantan-2-yl-2-(4-chloro-phenyl)-acetamide;-   (2,4-Dichloro-phenyl)-(3-methyl-piperidin-1-yl)-methanone;-   2-(4-tert-Butyl-phenoxy)-N-cyclooctyl-acetamide;-   (10,11-Dihydro-dibenzo[b,f]azepin-5-yl)-(2-methoxy-phenyl)-methanone;-   (3-Chloro-phenyl)-(2-methyl-piperidin-1-yl)-methanone;-   (3-Chloro-6-nitro-benzo[b]thiophen-2-yl)-(3-methyl-piperidin-1-yl)-methanone;-   (2,5-Dichloro-phenyl)-(4-methyl-piperidin-1-yl)-methanone;-   N-[5-(3,4-Dichloro-benzyl)-[1,3,4]thiadiazol-2-yl]-2,2-dimethyl-propionamide;-   4-(4-Chloro-2-methyl-phenoxy)-1-(3,4-dihydro-2H-quinolin-1-yl)-butan-1-one;-   (3,4-Dichloro-phenyl)-[4-(2,3-dimethyl-phenyl)-piperazin-1-yl]-methanone;-   Cyclooctanecarboxylic acid    [1-(naphthalene-2-sulfonyl)-pyrrolidin-2-yl]-amide;-   1-Butyl-pyrrolidine-2-carboxylic acid benzo[1,3]dioxol-4-ylamide;-   5-Methyl-furan-2-carboxylic acid dibenzylamide;-   (3,4-Dihydro-2H-quinolin-1-yl)-[3-(4-phenyl-piperazine-1-sulfonyl)-phenyl]-methanone;-   Bicyclo[2.2.1]hept-2-yl-[4-(2,3-dimethyl-phenyl)-piperazin-1-yl]-methanone;-   N-Adamantan-1-yl-2-benzoyl-benzamide;-   [5-(2-Chloro-phenoxymethyl)-furan-2-yl]-(3-methyl-piperidin-1-yl)-methanone;-   (3,5-Dimethyl-piperidin-1-yl)-(2-iodo-phenyl)-methanone;-   1-Benzenesulfonyl-pyrrolidine-2-carboxylic acid cyclooctylamide;-   (3,4-Dimethoxy-phenyl)-(6-fluoro-2-methyl-3,4-dihydro-2H-quinolin-1-yl)-methanone;-   3-(2,6-Dichloro-phenyl)-1-(2-ethyl-piperidin-1-yl)-propenone;-   N-(3,4-Difluoro-phenyl)-2,6-difluoro-benzamide;-   2,6-Difluoro-N-naphthalen-1-yl-benzamide;-   (4-Chloro-phenyl)-(3,5-dimethyl-piperidin-1-yl)-methanone;-   N-[4-(2,6-Dimethyl-piperidine-1-carbonyl)-phenyl]-2-(naphthalen-2-yloxy)-acetamide;-   (2-Chloro-phenyl)-(3-methyl-piperidin-1-yl)-methanone;-   N-{2-[4-(Piperidine-1-sulfonyl)-phenyl]-ethyl}-acetamide;-   N-Biphenyl-2-yl-2-(pyridin-2-ylsulfanyl)-acetamide;-   Azepan-1-yl-[5-(4-chloro-3,5-dimethyl-pyrazol-1-ylmethyl)-furan-2-yl]-methanone;-   Acetic acid 4-(4-methyl-piperidine-1-carbonyl)-phenyl ester;-   Acetic acid 4-(4-benzyl-piperidine-1-carbonyl)-phenyl ester;-   Benzo[1,3]dioxole-5-carboxylic acid cycloheptylamide;-   2-(2,4-Dimethyl-phenoxy)-1-(6-fluoro-2-methyl-3,4-dihydro-2H-quinolin-1-yl)-ethanone;-   Acetic acid 4-(3,4-dihydro-2H-quinoline-1-carbonyl)-phenyl ester;-   Azepan-1-yl-(3,5-dibromo-phenyl)-methanone;-   (3,5-Dibromo-phenyl)-[4-(2-methoxy-phenyl)-piperazin-1-yl]-methanone;-   N-Cyclooctyl-4-isopropyl-benzamide;-   N-Cyclooctyl-2-(4-methoxy-phenyl)-acetamide;-   (4-tert-Butyl-piperidin-1-yl)-phenyl-methanone;-   N-(4-tert-Butyl-3-nitro-phenyl)-acetamide;-   (2,6-Dimethyl-piperidin-1-yl)-[5-(2,3,5,6-tetrafluoro-phenoxymethyl)-furan-2-yl]-methanone;-   N-Cyclohexyl-3-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-N-methyl-propionamide;-   2-(4-Chloro-3-methyl-phenoxy)-N-cyclohexyl-N-methyl-acetamide;-   N-Cyclopentyl-3-(3,4-dihydro-2H-quinoline-1-carbonyl)-benzenesulfonamide;-   (3,4-Dihydro-1H-isoquinolin-2-yl)-(3-dimethylamino-phenyl)-methanone;-   3-Cyclohexylcarbamoyl-bicyclo[2.2.1]hept-5-ene-2-carboxylic acid    isopropyl ester;-   1-(3,4-Dihydro-1H-isoquinolin-2-yl)-2-(2-methoxy-phenyl)-ethanone;-   N-Benzyl-N-cyclohex-1-enyl-benzamide;-   [1-(Thiophene-2-sulfonyl)-piperidin-4-yl]-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone;-   N-Adamantan-1-yl-2-(1-phenyl-1H-tetrazol-5-ylsulfanyl)-acetamide;-   (3,4-Dihydro-2H-quinolin-1-yl)-[4-(morpholine-4-sulfonyl)-phenyl]-methanone;-   (3,4-Dihydro-2H-quinolin-1-yl)-[4-(pyrrolidine-1-sulfonyl)-phenyl]-methanone;-   (3,4-Dihydro-2H-quinolin-1-yl)-[1-(thiophene-2-sulfonyl)-piperidin-4-yl]-methanone;-   (1-Benzenesulfonyl-piperidin-3-yl)-(3,4-dihydro-1H-isoquinolin-2-yl)-methanone;-   6,7-Dimethyl-4-oxa-tricyclo[4.3.0.0^(3,7)]nonane-3-carboxylic acid    cyclohexylamide;-   6,7-Dimethyl-4-oxa-tricyclo[4.3.0.0^(3,7)]nonane-3-carboxylic acid    (2-chloro-phenyl)-amide;-   (6,7-Dimethyl-4-oxa-tricyclo[4.3.0.0^(3,7)]non-3-yl)-piperidin-1-yl-methanone;-   2-(5,6-Dimethyl-4-oxo-3,4-dihydro-thieno[2,3-d]pyrimidin-2-ylsulfanyl)-N-furan-2-ylmethyl-acetamide;-   N-Allyl-2-(5,6-dimethyl-4-oxo-3,4-dihydro-thieno[2,3-d]pyrimidin-2-ylsulfanyl)-acetamide;-   N-Adamantan-1-yl-2-(5,6,7,8-tetrahydro-benzo[4,5]thieno[2,3-d]pyrimidin-4-ylsulfanyl)acetamide;-   1-(3,4-Dihydro-2H-quinoline-1-carbonyl)-4,7,7-trimethyl-2-oxa-bicyclo[2.2.1]heptan-3-one;-   1-(3,4-Dihydro-1H-isoquinoline-2-carbonyl)-4,7,7-trimethyl-2-oxa-bicyclo[2.2.1]heptan-3-one;-   Azepan-1-yl-(6,7-dimethyl-4-oxa-tricyclo[4.3.0.0^(3,7)]non-3-yl)-methanone;-   2,5-Dimethyl-furan-3-carboxylic acid (1-adamantan-1-yl-ethyl)-amide;-   1-Cyclohexyl-5-oxo-pyrrolidine-3-carboxylic acid    (3-cyano-4,5,6,7-tetrahydro-benzo[b]thiophen-2-yl)-amide;-   2-(2-Cyano-phenylsulfanyl)-N-cyclopentyl-benzamide;-   [5-(2-Methoxy-4-propyl-phenoxymethyl)-furan-2-yl]-(3-methyl-piperidin-1-yl)-methanone;-   (4-tert-Butyl-phenyl)-(3,5-dimethyl-piperidin-1-yl)-methanone;-   [4-(2-Methoxy-naphthalen-1-ylmethyl)-piperazin-1-yl]-(4-methoxy-phenyl)-methanone;-   (3,4-Dichloro-phenyl)-(3,5-dimethyl-piperidin-1-yl)-methanone;-   (4-Ethoxy-phenyl)-(4-methyl-piperidin-1-yl)-methanone;-   2-Phenethyl-N-(tetrahydro-furan-2-ylmethyl)-benzamide;-   N-Cycloheptyl-2-phenoxy-benzamide;-   Adamantane-1-carboxylic acid (2-ethoxy-phenyl)-amide;-   N-Adamantan-2-yl-2-o-tolyloxy-acetamide;-   (2-Chloro-phenyl)-(3,5-dimethyl-piperidin-1-yl)-methanone;-   1-Morpholin-4-yl-2-[3-(4-nitro-phenyl)-adamantan-1-yl]-ethanone;-   2-Dimethylamino-N-(2-nitro-phenyl)-benzamide;-   N-Benzyl-2-(4,4,6-trimethyl-1-p-tolyl-1,4-dihydro-pyrimidin-2-ylsulfanyl)-acetamide;-   [4-(3,5-Dinitro-phenoxy)-phenyl]-(2-ethyl-piperidin-1-yl)-methanone;-   1-(4-Chloro-benzoyl)-2,3-dihydro-1H-benzo[g]quinolin-4-one;-   2-[(Adamantane-1-carbonyl)-amino]-3-phenyl-propionic acid methyl    ester;-   [Benzyl-(4-nitro-benzoyl)-amino]-acetic acid ethyl ester;-   9-Oxo-9H-fluorene-3-carboxylic acid methyl-(4-nitro-phenyl)-amide;-   Adamantane-1-carboxylic acid [2-(4-methoxy-phenyl)-ethyl]-amide;-   (10,11-Dihydro-dibenzo[b,f]azepin-5-yl)-(4-fluoro-phenyl)-methanone;-   2-Benzylsulfanyl-N-[2-(2-methoxy-phenoxy)-ethyl]-acetamide;-   N-Adamantan-1-yl-2-(2-oxo-4-phenyl-pyrrolidin-1-yl)-acetamide;-   2-Bromo-N-tricyclo[3.2.1.0^(2,4)]oct-6-ylmethyl-benzamide;-   Adamantane-1-carboxylic acid (2,6-dimethoxy-pyrimidin-4-yl)-amide;-   Hexanedioic acid    (2,7,7-trimethyl-bicyclo[2.2.1]hept-1-yl)-amide(1,7,7-trimethyl-bicyclo[2.2.1]hept-2-yl)-amide;-   2-Chloro-N-(2-cyclohexyl-ethyl)-benzamide;-   2-[3-(2-Ethyl-piperidin-1-yl)-3-oxo-propyl]-isoindole-1,3-dione;-   N-Adamantan-1-yl-2-hydroxy-2,2-diphenyl-acetamide;-   Adamantane-1-carboxylic acid (naphthalen-1-ylmethyl)-amide;-   Adamantane-1-carboxylic acid (benzo[1,3]dioxol-5-ylmethyl)-amide;-   1-(Azepane-1-carbonyl)-fluoren-9-one;-   2-(Quinolin-2-ylsulfanyl)-N-p-tolyl-acetamide;-   2,4-Dichloro-N-[3-(piperidine-1-carbonyl)-phenyl]-benzamide;-   2-Chloro-4,5-difluoro-N-(3,3,5-trimethyl-cyclohexyl)-benzamide;-   2-(2-Chloro-benzylsulfanyl)-N-p-tolyl-acetamide;-   [4-(4-Chloro-phenylsulfanylmethyl)-phenyl]-pyrrolidin-1-yl-methanone;-   N-Adamantan-1-yl-N-methyl-isonicotinamide;-   Azepan-1-yl-[4-(4-chloro-phenylsulfanylmethyl)-phenyl]-methanone;-   (2-Chloro-phenyl)-(1,5,7-trimethyl-3,7-diaza-bicyclo[3.3.1]non-3-yl)-methanone;-   (3-Chloro-benzo[b]thiophen-2-yl)-(4-methyl-piperidin-1-yl)-methanone;-   Benzoic acid 1-benzoyl-decahydro-quinolin-4-yl ester;-   2-(3-Bromo-benzylsulfanyl)-1-[4-(2-methoxy-phenyl)-piperazin-1-yl]-ethanone;-   4-Methyl-N-[2-(phenoxazine-10-carbonyl)-phenyl]-benzenesulfonamide;-   2-[1-(Azepane-1-carbonyl)-2-methyl-propyl]-isoindole-1,3-dione;-   2-(3-Bromo-benzylsulfanyl)-1-piperidin-1-yl-ethanone;-   1-[3-(4-Bromo-phenyl)-1-furan-2-yl-3-oxo-propyl]-pyrrolidin-2-one;-   2-Chloro-N-cyclooctyl-4,5-difluoro-benzamide;-   2,4-Dichloro-N-(2-furan-2-ylmethyl-cyclohexyl)-benzamide;-   N-(4-Benzoyl-furazan-3-yl)-2-fluoro-benzamide;-   N-Adamantan-1-yl-2-(3-cyano-4-methoxymethyl-6-methyl-pyridin-2-ylsulfanyl)-acetamide;-   4-tert-Butyl-N-cyclooctyl-benzamide;-   N-Adamantan-1-yl-2-phenyl-butyramide;-   (3-Chloro-6-methoxy-benzo[b]thiophen-2-yl)-piperidin-1-yl-methanone;-   (3,7-Dichloro-6-methoxy-benzo[b]thiophen-2-yl)-piperidin-1-yl-methanone;-   Acetic acid 1-benzoyl-decahydro-quinolin-4-yl ester;-   2-Bromo-N-methyl-N-phenyl-benzamide;-   N-Benzo[1,3]dioxol-5-yl-2,4-dichloro-benzamide;-   (3-Chloro-6-fluoro-benzo[b]thiophen-2-yl)-piperidin-1-yl-methanone;-   N-(1,2,3,5,6,7-Hexahydro-s-indacen-1-yl)-2-piperidin-1-yl-acetamide;-   2-[2-(1,3-Dioxo-1,3-dihydro-isoindol-2-yl)-3-phenyl-propionylamino]-3-methyl-butyric    acid methyl ester;-   2-(6-Oxo-6-piperidin-1-yl-hexyl)-isoindole-1,3-dione;-   2-[2-(1,3-Dioxo-1,3-dihydro-isoindol-2-yl)-3-phenyl-propionylamino]-3-methyl-butyric    acid methyl ester;-   Adamantane-1-carboxylic acid (2,6-dihydroxy-pyrimidin-4-yl)-amide;-   Adamantane-1-carboxylic acid methyl-phenyl-amide;-   3-Chloro-benzo[b]thiophene-2-carboxylic acid dibenzylamide;-   N-Adamantan-1-yl-2-(3-cyano-6-methyl-4-trifluoromethyl-pyridin-2-ylsulfanyl)-acetamide;-   2-(3-Oxo-3-phenyl-propenyl)-isoindole-1,3-dione;-   N-[5-(5-Chloro-benzooxazol-2-yl)-2-methyl-phenyl]-2-methoxy-benzamide;-   N-[2-(2-Bromo-phenyl)-benzooxazol-5-yl]-2-methoxy-benzamide;-   2-(4-Chloro-phenoxy)-N-(4-chloro-3-trifluoromethyl-phenyl)-acetamide;-   2,2-Dimethyl-N-(5-propyl-[1,3,4]thiadiazol-2-yl)-propionamide;-   2-[2-(2,6-Dimethyl-morpholin-4-yl)-1-methyl-2-oxo-ethyl]-isoindole-1,3-dione;-   2-(2-Cyano-phenylsulfanyl)-N-(2-trifluoromethyl-phenyl)-benzamide;-   Azepan-1-yl-(3,6-dichloro-benzo[b]thiophen-2-yl)-methanone;-   Benzo[1,3]dioxol-5-yl-(4-benzyl-piperidin-1-yl)-methanone;-   Azepan-1-yl-(3-chloro-6-methyl-benzo[b]thiophen-2-yl)-methanone;-   N-(5-Hexyl-[1,3,4]thiadiazol-2-yl)-isobutyramide;-   (3-Chloro-phenyl)-(10,11-dihydro-dibenzo[b,f]azepin-5-yl)-methanone;-   (2-Chloro-phenyl)-(10,11-dihydro-dibenzo[b,f]azepin-5-yl)-methanone;-   2-Amino-5-(azepane-1-carbonyl)-4-methyl-thiophene-3-carboxylic acid    ethyl ester;-   Adamantan-1-yl-(4-cyclopropyl-1,4,6,7-tetrahydro-imidazo[4,5-c]pyridin-5-yl)-methanone;-   Adamantan-1-yl-(4-trifluoromethyl-1,4,6,7-tetrahydro-imidazo[4,5-c]pyridin-5-yl)-methanone;-   Adamantan-1-yl-[4-(1H-benzoimidazol-2-ylsulfanyl)-piperidin-1-yl]-methanone;-   Adamantan-1-yl-(1,4,6,7-tetrahydro-imidazo[4,5-c]pyridin-5-yl)-methanone;-   [4-(1H-Imidazol-4-yl)-piperidin-1-yl]-(4-pentyl-phenyl)-methanone;-   3-Cyclohexyl-1-[4-(1H-imidazol-4-yl)-piperidin-1-yl]-propan-1-one;-   1-(4-Propyl-piperazin-1-yl)-3-(4-trifluoromethyl-phenyl)-propan-1-one;-   N-(2-Hydroxy-benzyl)-3-thiophen-3-yl-N-(2-thiophen-2-yl-ethyl)-acrylamide;-   N-(1,3-Dimethyl-pentyl)-2-(3-fluoro-phenyl)-N-(4-hydroxy-benzyl)-acetamide;-   N-Cyclobutyl-2-(3-fluoro-phenyl)-N-(4-hydroxy-benzyl)-acetamide;-   N-Cyclobutyl-N-(4-hydroxy-benzyl)-4-trifluoromethyl-benzamide;-   N-(3-Hydroxy-benzyl)-2-methyl-3-nitro-N-(4-sulfamoyl-benzyl)-benzamide;-   N-(4-Bromo-benzyl)-N-(4-hydroxy-benzyl)-2-naphthalen-1-yl-acetamide;-   6-(2-Bromo-phenylsulfanyl)-hexanoic acid    (3-amino-2,2-dimethyl-propyl)-amide;-   N-(3-Amino-2,2-dimethyl-propyl)-4-[2-(2-isopropyl-phenylsulfanyl)-ethyl]-benzamide;-   N-(3-Amino-2,2-dimethyl-propyl)-4-[4-(4-chloro-phenyl)-pyrimidin-2-ylsulfanylmethyl]-3-nitro-benzamide;-   4-(4-Bromo-phenyl)-N-(2-hydroxy-benzyl)-4-oxo-N-thiophen-2-ylmethyl-butyramide;-   N-[2-(2,4-Dichloro-phenyl)-ethyl]-N-(4-hydroxy-benzyl)-2-thiophen-3-yl-acetamide;-   N-(2-Chloro-benzyl)-N-(4-hydroxy-benzyl)-2-thiophen-2-yl-acetamide;-   Heptanoic acid benzyl-(4-hydroxy-benzyl)-amide;-   N-(4-Fluoro-benzyl)-N-(4-hydroxy-benzyl)-2-thiophen-3-yl-acetamide;-   4-Methyl-pentanoic acid (4-fluoro-benzyl)-(4-hydroxy-benzyl)-amide;-   N-Allyl-2-(4-chloro-phenyl)-N-(4-hydroxy-benzyl)-acetamide;-   N-Allyl-2-benzo[b]thiophen-3-yl-N-(4-hydroxy-benzyl)-acetamide;-   Heptanoic acid (3-ethoxy-propyl)-(4-hydroxy-benzyl)-amide;-   Dec-3-enoic acid    (4-hydroxy-benzyl)-(4-trifluoromethyl-benzyl)-amide;-   6-Oxo-6-phenyl-hexanoic acid    (4-hydroxy-benzyl)-(4-trifluoromethyl-benzyl)-amide;-   2-(3,4-Difluoro-phenyl)-N-(4-hydroxy-benzyl)-N-thiophen-2-ylmethyl-acetamide;-   2-Methyl-pent-4-enoic acid    (3-hydroxy-benzyl)-[2-(2-methoxy-phenyl)-ethyl]-amide;-   Heptanoic acid (3-hydroxy-benzyl)-(4-isopropyl-benzyl)-amide;-   5-(2,6-Dichloro-phenylsulfanyl)-pentanoic acid    (naphthalen-1-ylmethyl)-amide;-   N-(6,6-Dimethyl-bicyclo[3.1.1]hept-2-ylmethyl)-4-[2-(5-methyl-1H-benzoimidazol-2-ylsulfanyl)ethyl]-benzamide;-   N-(6,6-Dimethyl-bicyclo[3.1.1]hept-2-ylmethyl)-4-[2-(4-phenoxy-pyrimidin-2-ylsulfanyl)-ethyl]-benzamide;-   N-(6,6-Dimethyl-bicyclo[3.1.1]hept-2-ylmethyl)-4-[2-(4-fluoro-phenylsulfanyl)-ethyl]-benzamide;-   4-(2,6-Dichloro-phenylsulfanyl)-N-(6,6-dimethyl-bicyclo[3.1.1]hept-2-ylmethyl)-butyramide;-   5-(3-Methylsulfanyl-[1,2,4]thiadiazol-5-ylsulfanyl)-pentanoic acid    (6,6-dimethyl-bicyclo[3.1.1]hept-2-ylmethyl)-amide;-   5-(2,6-Dichloro-phenylsulfanyl)-pentanoic acid    [2-(3-trifluoromethyl-phenyl)-ethyl]-amide;-   4-[2-(2,6-Dichloro-phenylsulfanyl)-ethyl]-N-[2-(2-fluoro-phenyl)-ethyl]-benzamide;-   2-Cyclohexylamino-thiazole-4-carboxylic acid    (1,2,3,4-tetrahydro-naphthalen-1-yl)-amide;-   2-Cyclohexylamino-thiazole-4-carboxylic acid    (3-chloro-4-hydroxy-phenyl)-amide;-   2-Cyclohexylamino-thiazole-4-carboxylic acid    (1,2-dimethyl-propyl)-amide;-   2-Cyclohexylamino-thiazole-4-carboxylic acid (1-ethyl-propyl)-amide;-   2-Cyclohexylamino-thiazole-4-carboxylic acid    [3-(1-hydroxy-ethyl)-phenyl]-amide;-   2-Cyclohexylamino-thiazole-4-carboxylic acid    (1-ethynyl-cyclohexyl)-amide;-   2-Cyclohexylamino-thiazole-4-carboxylic acid    (2-methoxy-dibenzofuran-3-yl)-amide;-   2-Cyclohexylamino-thiazole-4-carboxylic acid    [2-(4-hydroxy-phenyl)-ethyl]-amide;-   2-Cyclohexylamino-thiazole-4-carboxylic acid    (4-hydroxy-cyclohexyl)-amide;-   2-(2,6-Difluoro-benzylamino)-N-[2-(3-trifluoromethyl-phenyl)-ethyl]-acetamide;-   4-{4-[2-(4-Dimethylamino-phenyl)-acetyl]-piperazin-1-yl}-3-(2-phenyl-propylamino)-benzamide;-   2-(2-Ethyl-phenylsulfanyl)-3-[methyl-(2-pyridin-4-yl-ethyl)-amino]-N-prop-2-ynyl-propionamide;-   4-Methyl-cyclohexanecarboxylic acid    {[2-(2-chloro-6-fluoro-benzylsulfanyl)-ethylcarbamoyl]-methyl}-prop-2-ynyl-amide;-   2-Benzylsulfanyl-N-{[2-(2-chloro-6-fluoro-benzylsulfanyl)-ethylcarbamoyl]-methyl}-N-(2-methoxyethyl)-acetamide;-   4-[2-(5-Cyclopropylmethylsulfanyl-[1,3,4]thiadiazol-2-ylsulfanyl)-ethyl]-N-(6,6-dimethyl-bicyclo[3.1.1]hept-2-ylmethyl)-benzamide;-   N-(6,6-Dimethyl-bicyclo[3.1.1]hept-2-ylmethyl)-2-p-tolyloxy-acetamide;-   Bicyclo[2.2.1]hept-5-ene-2-carboxylic acid    [4-(2,5-difluoro-phenoxy)-butyl]-amide;-   4-Trifluoromethyl-cyclohexanecarboxylic acid    [6-(2,6-difluoro-phenoxy)-hexyl]-amide;-   N-Cyclopropyl-3-methoxy-N-(2-piperidin-4-yl-ethyl)-5-(pyridine-2-carbonyl)-benzamide;-   3-Methoxy-N-(2-methoxy-ethyl)-N-(2-piperidin-4-yl-ethyl)-5-(pyridine-2-carbonyl)-benzamide;-   3-Methoxy-N-(2-piperidin-4-yl-ethyl)-5-(pyridine-2-carbonyl)-N-(tetrahydro-furan-2-ylmethyl)benzamide;-   3-Methoxy-N-(2-oxo-azepan-3-yl)-N-(2-piperidin-4-yl-ethyl)-5-(pyridine-2-carbonyl)-benzamide;-   3-Methoxy-N-[3-(2-oxo-pyrrolidin-1-yl)-propyl]-N-(2-piperidin-4-yl-ethyl)-5-(pyridine-2-carbonyl)benzamide;-   3-Methoxy-N-methyl-N-(2-piperidin-4-yl-ethyl)-5-(pyridine-2-carbonyl)-benzamide;-   [2-({Cyclopropyl-[3-methoxy-5-(pyridine-2-carbonyl)-benzoyl]-amino}-methyl)-phenoxy]-acetic    acid;-   (2-{[[3-Methoxy-5-(pyridine-2-carbonyl)-benzoyl]-(3-methyl-butyl)-amino]-methyl}-phenoxy)acetic    acid;-   [2-({Cyclopentyl-[3-methoxy-5-(pyridine-2-carbonyl)-benzoyl]-amino}-methyl)-phenoxy]-acetic    acid;-   [2-({(2-Methoxy-ethyl)-[3-methoxy-5-(pyridine-2-carbonyl)-benzoyl]-amino}-methyl)-phenoxy]-acetic    acid;-   [2-({Carbamoylmethyl-[3-methoxy-5-(pyridine-2-carbonyl)-benzoyl]-amino}-methyl)-phenoxy]-acetic    acid;-   [2-({[3-Methoxy-5-(pyridine-2-carbonyl)-benzoyl]-pyridin-4-yl-amino}-methyl)-phenoxy]-acetic    acid;-   [2-({Cyclopropylmethyl-[3-methoxy-5-(pyridine-2-carbonyl)-benzoyl]-amino}-methyl)-phenoxy]-acetic    acid;-   [2-({[3-Methoxy-5-(pyridine-2-carbonyl)-benzoyl]-methyl-amino}-methyl)-phenoxy]-acetic    acid;-   [4-(4-Hydroxy-benzyl)-piperazin-1-yl]-[3-methoxy-5-(pyridine-2-carbonyl)-phenyl]-methanone;-   {Carbamoylmethyl-[3-methoxy-5-(pyridine-2-carbonyl)-benzoyl]-amino}-acetic    acid;-   {(3-Imidazol-1-yl-propyl)-[3-methoxy-5-(pyridine-2-carbonyl)-benzoyl]-amino}-acetic    acid;-   {[3-Methoxy-5-(pyridine-2-carbonyl)-benzoyl]-pyridin-4-yl-amino}-acetic    acid;-   [[3-Methoxy-5-(pyridine-2-carbonyl)-benzoyl]-(2-oxo-azepan-3-yl)-amino]-acetic    acid;-   3-Methoxy-N-(2-methoxy-ethyl)-N-piperidin-3-ylmethyl-5-(pyridine-2-carbonyl)-benzamide;-   4-[3-Methoxy-5-(pyridine-2-carbonyl)-benzoylamino]-piperidine-1-carboxylic    acid ethyl ester;-   3-Methoxy-N-[3-(2-oxo-pyrrolidin-1-yl)-propyl]-5-(pyridine-2-carbonyl)-benzamide;-   3-({Carbamoylmethyl-[3-methoxy-5-(pyridine-2-carbonyl)-benzoyl]-amino}-methyl)-benzoic    acid;-   3-({(3-Imidazol-1-yl-propyl)-[3-methoxy-5-(pyridine-2-carbonyl)-benzoyl]-amino}-methyl)-benzoic    acid;-   4-Amino-N-(3-hydroxy-benzyl)-N-indan-2-yl-2-propionylamino-butyramide;-   5-Amino-2-propionylamino-pentanoic acid    (3-hydroxy-benzyl)-indan-2-yl-amide;-   N-Ethyl-2-hexylamino-N-(4-hydroxy-benzyl)-acetamide;-   2-Hexylamino-N-(4-hydroxy-benzyl)-N-methyl-acetamide;-   1-[1-(6-Phenyl-hexanoyl)-piperidin-4-yl]-1,3-dihydro-benzoimidazol-2-one;-   1-[1-(3-Cyclohexyl-propionyl)-piperidin-4-yl]-1,3-dihydro-benzoimidazol-2-one;-   N-(2-Hydroxy-benzyl)-N-isobutyl-benzamide;-   N-(2-Hydroxy-benzyl)-2-(4-hydroxy-phenyl)-N-isobutyl-acetamide;-   N-(2-Hydroxy-benzyl)-N-(3-methyl-butyl)-benzamide;-   N-(4-Hydroxy-benzyl)-N-isobutyl-benzamide;-   4-Hydroxy-N-(4-hydroxy-benzyl)-N-isobutyl-benzamide;-   N-(4-Hydroxy-benzyl)-2-(4-hydroxy-phenyl)-N-isobutyl-acetamide;-   N-(4-Hydroxy-benzyl)-N-(3-methyl-butyl)-benzamide;-   N-(2-Ethoxy-ethyl)-4-hydroxy-N-(4-hydroxy-benzyl)-benzamide;-   N-(4-Hydroxy-benzyl)-N-(3-isopropoxy-propyl)-benzamide;-   N-(3-Hydroxy-benzyl)-N-(4-methyl-pentyl)-benzamide;-   N-(3-Hydroxy-benzyl)-2-(4-hydroxy-phenyl)-N-(4-methyl-pentyl)-acetamide;-   N-(3-Hydroxy-benzyl)-N-(3-isopropoxy-propyl)-benzamide;-   N-(2-Hydroxy-benzyl)-N-(3-methyl-butyl)-4-propyl-benzamide;-   N-(4-Hydroxy-benzyl)-N-(6-hydroxy-hexyl)-4-propyl-benzamide;-   N-(4-Hydroxy-benzyl)-N-(3-methyl-butyl)-4-propyl-benzamide;-   N-[2-(4-Fluoro-benzylamino)-thiazol-4-ylmethyl]-N-phenethyl-butyramide;    or    a salt thereof with a pharmaceutically acceptable acid or base, or    any optical isomer or mixture of optical isomers, including a    racemic mixture, or any tautomeric forms.

In another embodiment, the present invention is concerned thesubstituted amides or prodrugs thereof of the general formula (II)

whereinR¹ is C₃-C₁₀cycloalkyl or C₃-C₁₀hetcycloalkyl, wherein the cycloalkyland hetcycloalkyl groups independently are optionally substituted withone or more of R⁴;R² is hydrogen, C₁-C₈alkyl, arylC₁-C₆alkyl, wherein the alkyl and arylgroups independently are optionally substituted with one or more of R⁵;orR¹ and R² together with the nitrogen to which they are attached, areforming a saturated or partially saturated cyclic, bicyclic or tricyclicring system containing from 4 to 10 carbon atoms and from 0 to 2additional heteroatoms selected from nitrogen, oxygen or sulphur, thering system optionally being substituted with at least one ofC₁-C₈alkyl, aryl, hetaryl, arylC₁-C₆alkyl, hetarylC₁-C₆alkyl, hydroxy,oxo, cyano, C₁-C₆alkyloxy, arylC₁-C₆alkyloxy, hetarylC₁-C₆alkyloxy,C₁-C₆alkyloxyC₁-C₆alkyl, C₁-C₆alkylcarbonyl, arylcarbonyl,hetarylcarbonyl, arylC₁-C₆alkylcarbonyl, hetarylC₁-C₆alkylcarbonyl,C₁-C₆alkylcarboxy, arylcarboxy or arylC₁-C₆alkylcarboxy wherein thealkyl and aryl groups independently are optionally substituted with oneor more of R¹⁴;R³ is C₃-C₁₀cycloalkyl, C₃-C₁₀hetcycloalkyl, aryl or hetaryl, whereinthe alkyl, cycloalkyl, hetcycloalkyl, aryl and hetaryl groupsindependently are optionally substituted with one or more of R⁷;R⁴ and R⁵ independently are hydrogen, hydroxy, oxo, cyano, halo,methylendioxo, NR⁸R⁹, C₁-C₈alkyl, C₁-C₆alkyloxy, trihalomethyl,trihalomethyloxy, C₃-C₁₀cycloalkyl, C₃-C₁₀hetcycloalkyl,C₃-C₁₀cycloalkenyl, aryl, hetaryl, hetarylSO_(n), arylC₁-C₆alkyloxy,hetarylC₁-C₆alkyloxy, C₁-C₆alkyl-R⁶—C₁-C₆alkyl,arylC₁-C₆alkyl-R⁶—C₁-C₆alkyl, C₁-C₆alkylcarbonyl, arylcarbonyl,arylC₁-C₆alkylcarbonyl, hetarylcarbonyl, hetarylC₁-C₆alkylcarbonyl,C₁-C₆alkylSO_(n), C₁-C₆alkylcarboxy, arylcarboxy, hetarylcarboxy,arylC₁-C₆alkylcarboxy or hetarylC₁-C₆alkylcarboxy wherein the alkyl,cycloalkyl, hetcycloalkyl, aryl and hetaryl groups independently areoptionally substituted with one or more of R¹⁵;R⁶ is oxygen, sulphur, SO_(n) or NR¹⁶;R⁷ is hydrogen, halo, hydroxy, cyano, nitro, COOR¹⁷, C₁-C₈alkyl,C₃-C₁₀cycloalkyl, C₃-C₁₀hetcycloalkyl, methylendioxo, trihalomethyl,trihalomethyloxy, aryl, arylC₁-C₆alkyl, C₁-C₆alkyloxy,C₁-C₆alkyloxyC₁-C₆alkyl, aryloxy, arylC₁-C₆alkyloxy, aryloxyC₁-C₆alkyl,arylC₁-C₆alkyloxyC₁-C₆alkyl, hetaryl, hetarylC₁-C₆alkyl, hetaryloxy,hetarylC₁-C₆alkyloxy, hetaryloxyC₁-C₆alkyl,hetarylC₁-C₆alkyl-oxyC₁-C₆alkyl, NR⁸R⁹, SO_(m)NR⁸R⁹,NR⁴R⁵carbonylC₁-C₆alkyl, arylthio, hetarylthio, R¹⁸-carbonylNR⁸,arylSO_(n), hetarylSO_(n), R¹⁹SO_(m)NR⁸, arylthioC₁-C₆alkyl,hetarylthioC₁-C₆alkyl or arylC₁-C₆alkylR⁶C₁-C₆alkyl; wherein the aryland hetaryl groups independently are optionally substituted with one ormore R¹⁰;R⁸ and R⁹ independently are hydrogen, C₁-C₈alkyl, aryl, hetaryl,C₁-C₆alkylSO_(m), arylSO_(m), arylC₁-C₆alkylSO_(m), arylC₁-C₆alkyl orhetarylC₁-C₆alkyl wherein the alkyl, aryl and hetaryl groupsindependently are optionally substituted with one or more of R¹¹; orR⁸ and R⁹ together with the nitrogen to which they are attached, areforming a saturated or partially saturated cyclic, bicyclic or tricyclicring system containing from 4 to 10 carbon atoms and from 0 to 2additional heteroatoms selected from nitrogen, oxygen or sulfur, thering system optionally being substituted with at least one halo, cyano,C₁-C₈alkyl, aryl, hetaryl, arylC₁-C₆alkyl, hetarylC₁-C₆alkyl, hydroxy,oxo, C₁-C₆alkyloxy, arylC₁-C₆alkyloxy, hetarylC₁-C₆alkyloxy,C₁-C₆alkyloxyC₁-C₆alkyl, C₁-C₆alkylcarbonyl, arylcarbonyl,hetarylcarbonyl, arylC₁-C₆alkylcarbonyl, hetarylC₁-C₆alkylcarbonyl,C₁-C₆alkylcarboxy, arylcarboxy, hetarylcarboxy, arylC₁-C₆alkylcarboxy orhetarylC₁-C₆alkylcarboxy;R¹⁰ and R¹¹ independently are hydrogen, hydroxy, oxo, halo, cyano,nitro, C₁-C₈alkyl, C₁-C₆alkyl-oxy, NR¹²R¹³, methylendioxo, trihalomethylor trihalomethyloxy;R¹² and R¹³ independently are hydrogen, C₁-C₈alkyl or arylC₁-C₆alkyl;R¹⁴ is hydrogen, halo, hydroxy, oxo, nitro, cyano, C₁-C₈alkyl,C₁-C₆alkyloxy or aryloxy;R¹⁵ is hydrogen, halo, hydroxy, oxo, nitro, cyano, CONR⁸R⁹ or COOR¹⁷;R¹⁶ is hydrogen, C₁-C₈alkyl, C₃-C₁₀cycloalkyl, C₃-C₁₀hetcycloalkyl,aryl, arylC₁-C₆alkyl, hetaryl, hetarylC₁-C₆alkyl, alkylcarbonyl,arylcarbonyl, arylC₁-C₆alkylcarbonyl, aryloxyC₁-C₆alkyl,hetaryloxyC₁-C₆alkyl, arylthioC₁-C₆alkyl or hetarylthioC₁-C₆alkyl;wherein the alkyl, cycloalkyl, hetcycloalkyl, aryl and hetaryl groupsindependently are optionally substituted with one or more of R¹⁰;R¹⁷ is hydrogen, C₁-C₈alkyl, aryl or arylC₁-C₆alkyl;R¹⁸ is C₁-C₆alkyl, C₂-C₆alkenyl, aryl, arylC₁-C₆alkyl, hetaryl,hetarylC₁-C₆alkyl, C₃-C₁₀cycloalkyl, C₃-C₁₀hetcycloalkyl, C₁-C₆alkyloxy,aryloxy, arylC₁-C₆alkyloxy, arylC₁-C₆alkyloxyC₁-C₆alkyl,hetarylC₁-C₆alkyloxyC₁-C₆alkyl, hetaryloxy, hetarylC₁-C₆alkyloxy orR⁸R⁹NC₁-C₆alkyl wherein the alkyl, alkenyl, cycloalkyl, hetcycloalkyl,aryl and hetaryl groups are optionally substituted with R¹⁵;R¹⁹ is C₁-C₆alkyl, C₃-C₁₀cycloalkyl, C₃-C₁₀hetcycloalkyl, aryl,arylC₁-C₆alkyl, hetaryl, hetarylC₁-C₆alkyl;m is 1 or 2;n is 0, 1 or 2; ora salt thereof with a pharmaceutically acceptable acid or base, or anyoptical isomer or mixture of optical isomers, including a racemicmixture, or any tautomeric forms.

In another embodiment of the present invention, in formula (II) R¹ isC₃-C₁₀cycloalkyl or C₃-C₁₀hetcycloalkyl, wherein the cycloalkyl andhetcycloalkyl groups independently are optionally substituted with oneor more of R⁴ as defined above.

In another embodiment of the present invention, in formula (II) R² ishydrogen or C₁-C₈alkyl, wherein the alkyl group is optionallysubstituted with one or more of R⁵ as defined above.

In another embodiment of the present invention, in formula (II) R¹ andR² together with the nitrogen to which they are attached, are forming asaturated or partially saturated cyclic, bicyclic or tricyclic ringsystem containing from 4 to 10 carbon atoms and from 0 to 2 additionalheteroatoms selected from nitrogen, oxygen or sulphur, the ring systemoptionally being substituted with at least one of C₁-C₈alkyl, aryl,hetaryl, arylC₁-C₆alkyl, hetarylC₁-C₆alkyl, hydroxy, oxo, cyano,C₁-C₆alkyloxy, arylC₁-C₆alkyloxy, hetarylC₁-C₆alkyloxy,C₁-C₆alkyloxyC₁-C₆alkyl, C₁-C₆alkylcarbonyl, arylcarbonyl,hetarylcarbonyl, arylC₁-C₆alkylcarbonyl, hetarylC₁-C₆alkylcarbonyl,C₁-C₆alkylcarboxy, arylcarboxy or arylC₁-C₆alkylcarboxy wherein thealkyl and aryl groups independently are optionally substituted with oneor more of R¹⁴; as defined above.

In another embodiment of the present invention, in formula (II) R¹ andR² together with the nitrogen to which they are attached are6-aza-bicyclo[3.2.1]octane.

In another embodiment of the present invention, in formula (II) R³ isaryl or hetaryl, wherein the aryl and hetaryl groups independently areoptionally substituted with one or more of R⁷ as defined above.

In another embodiment of the present invention, in formula (II) R³ isC₃-C₁₀cycloalkyl or C₃-C₁₀hetcycloalkyl, optionally substituted with oneor more of R⁷ as defined above.

In another embodiment of the present invention, in formula (II) R⁴ andR⁵ independently are hydrogen, hydroxy, oxo, halo, C₁-C₈alkyl, whereinthe alkyl group is optionally substituted with one or more of R¹⁵ asdefined above.

In another embodiment of the present invention, in formula (II) R⁷ ishydrogen, halo, hydroxy, cyano, C₁-C₈alkyl, C₃-C₁₀cycloalkyl,C₃-C₁₀hetcycloalkyl, trihalomethyl, aryl, arylC₁-C₆alkyl, C₁-C₆alkyloxy,C₁-C₆alkyloxyC₁-C₆alkyl, aryloxy, arylC₁-C₆alkyloxy, aryloxyC₁-C₆alkyl,arylC₁-C₆alkyloxyC₁-C₆alkyl, hetaryl, hetarylC₁-C₆alkyl, hetaryloxy,hetarylC₁-C₆alkyloxy, hetaryloxyC₁-C₆alkyl,hetarylC₁-C₆alkyl-oxyC₁-C₆alkyl, NR⁸R⁹, R¹⁸-carbonylNR⁸, orR¹⁹SO_(m)NR⁸, wherein the aryl and hetaryl groups independently areoptionally substituted with one or more R¹⁰ as defined above.

In another embodiment of the present invention, in formula (II) R⁷ ishalo, cyano, C₁-C₈alkyl, C₃-C₁₀hetcycloalkyl, trihalomethyl, aryl,C₁-C₆alkyloxy, aryloxy, arylC₁-C₆alkyloxy, aryloxyC₁-C₆alkyl,arylC₁-C₆alkyloxyC₁-C₆alkyl, hetaryl, hetaryloxy, hetarylC₁-C₆alkyloxy,hetaryloxyC₁-C₆alkyl, hetarylC₁-C₆alkyloxyC₁-C₆alkyl, NR⁸R⁹,R⁸-carbonylNR⁸, or R¹⁹SO_(m)NR⁸, wherein the aryl and hetaryl groups areindependently optionally substituted with one or more R¹⁰ as definedabove.

In another embodiment of the present invention, in formula (II) R⁷ isR¹⁸-carbonylNR⁸ or R¹⁹SO_(m)NR⁸; wherein m, R⁸, R¹⁸ and R¹⁹ are definedas above.

In another embodiment of the present invention, in formula (II) R⁸ isC₁-C₆alkyl.

In another embodiment of the present invention, in formula (II) R⁸ andR⁹ together with the nitrogen to which they are attached, are forming asaturated or partially saturated cyclic, bicyclic or tricyclic ringsystem containing from 4 to 10 carbon atoms and from 0 to 2 additionalheteroatoms selected from nitrogen, oxygen or sulfur, the ring systemoptionally being substituted with at least one halo, cyano, C₁-C₈alkyl,aryl, hetaryl, arylC₁-C₆alkyl, hetarylC₁-C₆alkyl, hydroxy, oxo,C₁-C₆alkyloxy, arylC₁-C₆alkyloxy, hetarylC₁-C₆alkyloxy,C₁-C₆alkyloxyC₁-C₆alkyl, C₁-C₆alkylcarbonyl, arylcarbonyl,hetarylcarbonyl, arylC₁-C₆alkylcarbonyl, hetarylC₁-C₆alkylcarbonyl,C₁-C₆alkylcarboxy, arylcarboxy, hetarylcarboxy, arylC₁-C₆alkylcarboxy orhetarylC₁-C₆alkylcarboxy.

In another embodiment of the present invention, in formula (II) R¹⁵ isCONR⁸R⁹.

In another embodiment of the present invention, in formula (II) R¹⁸ isC₁-C₆alkyl, optionally substituted with R¹⁵ as defined above.

In another embodiment of the present invention, in formula (II) R¹⁸ isaryl or hetaryl.

In another embodiment of the present invention, in formula (II) R¹⁸ isarylC₁-C₆alkyloxyC₁-C₆alkyl or hetarylC₁-C₆alkyloxyC₁-C₆alkyl.

In another embodiment of the present invention, in formula (II) R¹⁸ isR⁸R⁹NC₁-C₆alkyl; wherein R⁸ and R⁹ are defined as above.

In another embodiment of the present invention, in formula (II) R¹⁹ isaryl or hetaryl

In another embodiment of the present invention, in formula (II) the arylgroup is phenyl or pyridyl.

In another embodiment of the present invention, in formula (II) thehetaryl group is thienyl, imidazolyl, oxazolyl, thiazolyl, or indolyl.

In another embodiment of the present invention, the compounds orprodrugs thereof of the general formula (II) are selected from the groupconsisting of the compounds of examples 4 through 8 as described underEXAMPLES, COMPOUNDS OF GENERAL FORMULAS (I) AND (II).

In another embodiment, the present invention concerns the substitutedamides or prodrugs thereof of the general formula (III)

whereinR¹ is aryl, arylC₁-C₆alkyl, hetaryl or hetarylC₁-C₆alkyl optionallysubstituted with one or more of R⁶ independently;R² is halo, C₁-C₆alkyl, C₂-C₆alkenyl, C₂-C₆alkynyl, C₃-C₁₀cycloalkyl,C₃-C₁₀cycloalkylC₁-C₆alkyl, trihalomethyl, aryl, arylC₁-C₆alkyl,C₁-C₆alkyloxyC₁-C₆alkyl, arylC₁-C₆alkyloxyC₁-C₆alkyl,C₁-C₆-alkylNR⁵C₁-C₆alkyl, arylC₁-C₆alkylNR⁵C₁-C₆alkyl, hetaryl orhetarylC₁-C₆alkyl wherein the alkyl, alkenyl, alkynyl, cycloalkyl andaryl groups independently are optionally substituted with one or moreR⁷;R³ is C₁-C₆alkyl optionally substituted with one or more of R⁸;R⁴ is C₆-C₁₀cycloalkyl, C₆-C₁₀hetcycloalkyl, C₆-C₁₀cycloalkylC₁-C₆alkylor C₆-C₁₀hetcycloalkylC₁-C₆alkyl wherein the alkyl, cycloalkyl andhetcycloalkyl groups independently are optionally substituted with oneor more of R⁸; orR³ and R⁴ together with the nitrogen to which they are attached, areforming a saturated or partially saturated bicyclic/bridge ring systemcontaining from 7 to 12 carbon atoms and from 0 to 2 additionalheteroatoms selected from nitrogen, oxygen or sulphur, the ring systemoptionally being substituted with at least one of C₁-C₆alkyl, aryl,hetaryl, arylC₁-C₆alkyl, hetarylC₁-C₆alkyl, hydroxy, oxo, C₁-C₆alkyloxy,arylC₁-C₆alkyloxy or hetarylC₁-C₆alkyloxy, wherein the alkyl and arylgroups independently are optionally substituted with one or more of R⁹;R⁵ is C₁-C₆alkyl, C₂-C₆alkenyl, C₂-C₆alkynyl, C₃-C₁₀cycloalkyl,C₃-C₁₀hetcycloalkyl, C₃-C₁₀-cycloalkylC₁-C₆alkyl,C₃-C₁₀hetcycloalkylC₁-C₆alkyl, aryl, hetaryl, arylC₁-C₆alkyl orhetarylC₁-C₆alkyl wherein the alkyl, alkenyl, alkynyl, aryl, hetaryl,cycloalkyl and hetcycloalkyl groups independently are optionallysubstituted with one or more of R⁹;R⁶ and R⁷ independently are hydrogen, hydroxy, oxo, halo, nitro, cyano,C₁-C₆alkyl, C₁-C₆-alkyloxy, trihalomethyl, trihalomethoxy, NR¹⁰R¹¹,arylC₁-C₆alkyloxy, hetarylC₁-C₆alkyloxy, C₁-C₆-alkylcarbonyl,arylcarbonyl, hetarylcarbonyl, arylC₁-C₆alkylcarbonyl,C₁-C₆alkyloxycarbonyl, aryloxycarbonyl, arylC₁-C₆alkyloxycarbonyl,C₁-C₆alkylcarboxy, arylcarboxy or arylC₁-C₆alkylcarboxy;R⁸ and R⁹ independently are hydrogen, C₁-C₆alkyl, aryl, hetaryl,arylC₁-C₆alkyl, hetarylC₁-C₆-alkyl, hydroxy, oxo, cyano, NR¹⁰R¹¹,C₁-C₆alkyloxy, aryloxy, arylC₁-C₆alkyloxy, hetaryloxy,hetarylC₁-C₆alkyloxy, C₁-C₆alkyloxyC₁-C₆alkyl, C₁-C₆alkylcarbonyl,arylcarbonyl, hetarylcarbonyl, arylC₁-C₆alkylcarbonyl,hetarylC₁-C₆alkylcarbonyl, C₁-C₆alkylcarboxy, arylcarboxy orarylC₁-C₆alkylcarboxy;R¹⁰ and R¹¹ independently are hydrogen, C₁-C₈alkyl, aryl, hetaryl,arylC₁-C₆alkyl, C₃-C₁₀-cycloalkyl, C₃-C₁₀hetcycloalkyl,C₃-C₁₀cycloalkylC₁-C₆alkyl, C₁-C₆alkylcarbonyl,C₁-C₆alkylcarboxyC₁-C₆alkyl; orR¹⁰ and R¹¹ together with the nitrogen to which they are attached, areforming a saturated or partially saturated cyclic, bicyclic or tricyclicring system containing from 4 to 10 carbon atoms and from 0 to 2additional heteroatoms selected from nitrogen, oxygen or sulphur, thering system optionally being substituted with at least one ofC₁-C₈alkyl, aryl, hetaryl, arylC₁-C₆alkyl, hetarylC₁-C₆alkyl, hydroxy,oxo, cyano, C₁-C₆alkyloxy, arylC₁-C₆alkyloxy, hetarylC₁-C₆alkyloxy,C₁-C₆alkyloxyC₁-C₆alkyl, C₁-C₆alkylcarbonyl, arylcarbonyl,hetarylcarbonyl, arylC₁-C₆alkylcarbonyl, hetarylC₁-C₆alkylcarbonyl,C₁-C₆alkylcarboxy, arylcarboxy or arylC₁₋₆-alkylcarboxy; ora salt thereof with a pharmaceutically acceptable acid or base, or anyoptical isomer or mixture of optical isomers, including a racemicmixture, or any tautomeric forms.

In another embodiment, the present invention is concerned with compoundsor prodrugs thereof of the general formula (III) wherein:

R¹ is aryl or hetaryl optionally substituted with one or more R⁶independently;

R² is halo, C₁-C₆alkyl, C₂-C₆alkenyl, C₂-C₆alkynyl, C₃-C₁₀cycloalkyl,C₃-C₁₀cycloalkylC₁-C₆alkyl, aryl, arylC₁-C₆alkyl,C₁-C₆alkyloxyC₁-C₆alkyl, arylC₁-C₆alkyloxyC₁-C₆alkyl,C₁-C₆alkylNR⁵C₁-C₆alkyl, arylC₁-C₆alkylNR⁵C₁-C₆alkyl, hetaryl orhetarylC₁-C₆alkyl wherein the alkyl, alkenyl, alkynyl, cycloalkyl andaryl groups independently are optionally substituted with one or moreR⁷;

R³ is C₁-C₆alkyl optionally substituted with one or more of R⁸;

R⁴ is C₆-C₁₀cycloalkyl, C₆-C₁₀hetcycloalkyl, C₆-C₁₀cycloalkylC₁-C₆alkylor C₆-C₁₀hetcycloalkylC₁-C₆alkyl wherein the alkyl, cycloalkyl andhetcycloalkyl groups independently are optionally substituted with oneor more of R⁸;

R⁵ is C₁-C₆alkyl, C₂-C₆alkenyl, C₂-C₆alkynyl, C₃-C₁₀cycloalkyl,C₃-C₁₀hetcycloalkyl, C₃-C₁₀-cycloalkylC₁-C₆alkyl,C₃-C₁₀hetcycloalkylC₁-C₆alkyl, aryl, hetaryl, arylC₁-C₆alkyl orhetarylC₁-C₆alkyl wherein the alkyl, alkenyl, alkynyl, aryl, hetaryl,cycloalkyl and hetcycloalkyl groups independently are optionallysubstituted with one or more of R⁹;

R⁶ and R⁷ independently are hydrogen, hydroxy, oxo, halo, nitro, cyano,C₁-C₆alkyl, C₁-C₆-alkyloxy, trihalomethyl, trihalomethoxy, NR¹⁰R¹¹,arylC₁-C₆alkyloxy, hetarylC₁-C₆alkyloxy, C₁-C₆-alkylcarbonyl,arylcarbonyl, hetarylcarbonyl, arylC₁-C₆alkylcarbonyl,C₁-C₆alkyloxycarbonyl, aryloxycarbonyl, arylC₁-C₆alkyloxycarbonyl,C₁-C₆alkylcarboxy, arylcarboxy or arylC₁-C₆alkylcarboxy;

R⁸ and R⁹ independently are hydrogen, C₁-C₆alkyl, aryl, hetaryl,arylC₁-C₆alkyl, hetarylC₁-C₆-alkyl, hydroxy, oxo, cyano, NR¹⁰R¹¹,C₁-C₆alkyloxy, aryloxy, arylC₁-C₆alkyloxy, hetaryloxy,hetarylC₁-C₆alkyloxy, C₁-C₆alkyloxyC₁-C₆alkyl, C₁-C₆alkyl-carbonyl,arylcarbonyl, hetarylcarbonyl, arylC₁-C₆alkylcarbonyl,hetarylC₁-C₆alkyl-carbonyl, C₁-C₆alkylcarboxy, arylcarboxy orarylC₁-C₆alkylcarboxy;

R¹⁰ and R¹¹ independently are hydrogen, C₁-C₈alkyl, aryl, hetaryl,arylC₁-C₆alkyl, C₃-C₁₀-cycloalkyl, C₃-C₁₀hetcycloalkyl,C₃-C₁₀cycloalkylC₁-C₆alkyl, C₁-C₆alkylcarboxyC₁-C₆alkyl; or

R¹⁰ and R¹¹ together with the nitrogen to which they are attached, areforming a saturated or partially saturated cyclic, bicyclic or tricyclicring system containing from 4 to 10 carbon atoms and from 0 to 2additional heteroatoms selected from nitrogen, oxygen or sulphur, thering system optionally being substituted with at least one ofC₁-C₈alkyl, aryl, hetaryl, arylC₁-C₆alkyl, hetarylC₁-C₆alkyl, hydroxy,oxo, cyano, C₁-C₆alkyloxy, arylC₁-C₆alkyloxy, hetaryl C₁-C₆alkyloxy,C₁-C₆alkyloxyC₁-C₆alkyl, C₁-C₆alkylcarbonyl, arylcarbonyl,hetarylcarbonyl, arylC₁-C₆alkylcarbonyl, hetarylC₁-C₆alkylcarbonyl,C₁-C₆alkylcarboxy, arylcarboxy or arylC₁₋₆-alkylcarboxy; or

a salt thereof with a pharmaceutically acceptable acid or base, or anyoptical isomer or mixture of optical isomers, including a racemicmixture, a prodrug thereof, or any tautomeric forms.

In another embodiment of the present invention, in formula (III) R¹ isaryl, arylC₁-C₆alkyl or hetaryl optionally substituted with one or moreof R⁶.

In another embodiment of the present invention, in formula (III) R¹ isaryl optionally substituted with one or more of R⁶.

In another embodiment of the present invention, in formula (III) R¹ isarylC₁-C₆alkyl optionally substituted with one or more of R⁶.

In another embodiment of the present invention, in formula (III) R¹ ishetaryl optionally substituted with one or more of R⁶.

In another embodiment of the present invention, in formula (III) R² isC₁-C₆alkyl, C₃-C₁₀cycloalkyl, C₃-C₁₀cycloalkylC₁-C₆alkyl, trihalomethyl,arylC₁-C₆alkyl, or hetarylC₁-C₆alkyl wherein the alkyl, cycloalkyl andaryl groups independently are optionally substituted with one or moreR⁷.

In another embodiment of the present invention, in formula (III) R² isC₁-C₆alkyl optionally substituted with one or more R⁷.

In another embodiment of the present invention, in formula (III) R² istrihalomethyl.

In another embodiment of the present invention, in formula (III) R³ isC₁-C₆alkyl optionally substituted with one or more of R⁸.

In another embodiment of the present invention, in formula (III) R⁴ isC₆-C₁₀cycloalkyl, or C₆-C₁₀hetcycloalkyl, wherein the cycloalkyl andhetcycloalkyl groups independently are optionally substituted with oneor more of R⁸.

In another embodiment of the present invention, in formula (III) R⁴ isC₆-C₁₀cycloalkyl optionally substituted with one or more of R⁸.

In another embodiment of the present invention, in formula (III) R⁴ isC₆C₆-C₁₀hetcycloalkyl optionally substituted with one or more of R⁸.

In another embodiment of the invention, in formula (III) R³ and R⁴together with the nitrogen to which they are attached, are forming asaturated or partially saturated bicyclic/bridge ring system containingfrom 7 to 12 carbon atoms and from 0 to 2 additional heteroatomsselected from nitrogen, oxygen or sulphur, the ring system optionallybeing substituted with at least one of C₁-C₆alkyl, aryl, hetaryl,arylC₁-C₆alkyl, hetarylC₁-C₆alkyl, hydroxy, oxo, C₁-C₆alkyloxy,arylC₁-C₆alkyloxy or hetarylC₁-C₆alkyloxy, wherein the alkyl and arylgroups independently are optionally substituted with one or more of R⁹.

In another embodiment of the present invention, in formula (III) thesaturated or partially saturated bicyclic/bridge ring system is6-aza-bicyclo[3.2.1]octane.

In another embodiment of the present invention, in formula (III) R⁶ andR⁷ independently are hydrogen, hydroxy, oxo, halo, cyano, C₁-C₆alkyl,C₁-C₆alkyloxy, trihalomethyl, NR¹⁰R¹¹, arylC₁-C₆alkyloxy,hetarylC₁-C₆alkyloxy, C₁-C₆alkylcarbonyl, arylcarbonyl, hetarylcarbonyl,arylC₁-C₆alkylcarbonyl, C₁-C₆alkyloxycarbonyl, aryloxycarbonyl orarylC₁-C₆alkyloxycarbonyl.

In another embodiment of the present invention, in formula (III) R⁸ andR⁹ independently are hydrogen, C₁-C₆alkyl, hydroxy, oxo, C₁-C₆alkyloxyor arylC₁-C₆alkyloxy.

In another embodiment of the present invention, in formula (III) R¹⁰ andR¹¹ independently are hydrogen or C₁-C₈alkyl.

In another embodiment of the present invention the compound of thegeneral formula (III) or a prodrug thereof is1-(4-Chloro-phenyl)-5-propyl-1H-pyrazole-4-carboxylic acidcyclohexyl-methyl-amide or a salt thereof with a pharmaceuticallyacceptable acid or base, or any optical isomer or mixture of opticalisomers, including a racemic mixture, or any tautomeric forms.

In another embodiment of the present invention the compounds of thegeneral formula (III) or a prodrug thereof is selected from the groupconsisting of:

-   1-(4-Chloro-phenyl)-5-trifluoromethyl-1H-pyrazole-4-carboxylic acid    cyclohexyl-methyl-amide;-   [1-(4-Methoxy-phenyl)-5-methyl-1H-pyrazol-4-yl]-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone;-   1    [1-(4-Chloro-phenyl)-5-propyl-1H-pyrazol-4-yl]-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone;-   [1-(3,5-Dichloro-phenyl)-5-propyl-1H-pyrazol-4-yl]-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone;    or    a salt thereof with a pharmaceutically acceptable acid or base, or    any optical isomer or mixture of optical isomers, including a    racemic mixture, or any tautomeric forms.

In yet another embodiment of the present invention the compounds of thegeneral formula (III) or a prodrug thereof is selected from the groupconsisting of:

-   1-(Phenyl)-5-methyl-1H-pyrazole-4-carboxylic acid    cyclohexyl-methyl-amide;-   1-(4-Fluoro-phenyl)-5-methyl-1H-pyrazole-4-carboxylic acid    cyclohexyl-methyl-amide;-   1-(4-Methoxy-phenyl)-5-methyl-1H-pyrazole-4-carboxylic acid    cyclohexyl-methyl-amide;-   1-(4-Chloro-phenyl)-5-methyl-1H-pyrazole-4-carboxylic acid    cyclohexyl-methyl-amide;-   1-(2-Methyl-phenyl)-5-methyl-1H-pyrazole-4-carboxylic acid    cyclohexyl-methyl-amide;-   1-(4-Amino-phenyl)-5-methyl-1H-pyrazole-4-carboxylic acid    cyclohexyl-methyl-amide;-   1-(2-Pyridyl)-5-methyl-1H-pyrazole-4-carboxylic acid    cyclohexyl-methyl-amide;-   1-(2-Pyridyl)-5-propyl-1H-pyrazole-4-carboxylic acid    cyclohexyl-methyl-amide; or    a salt thereof with a pharmaceutically acceptable acid or base, or    any optical isomer or mixture of optical isomers, including a    racemic mixture, or any tautomeric forms.

In another embodiment, the present invention is concerned with compoundsor prodrugs thereof of the general formula (IV)

whereinR¹ is hydrogen, trihalomethyl, C₁-C₆alkyl, C₁-C₆alkyloxy,C₁-C₆alkylthio, aryl, arylC₁-C₆alkyl, hetaryl or hetaralkyl, wherein thealkyl, aryl and hetaryl groups independently are optionally substitutedwith one or more of R⁸;R², R³, R⁴ and R⁵ independently are hydrogen, halo, nitro, cyano,hydroxy, NR⁹R¹⁰, trihalomethyl, C₁-C₆alkyl, C₁-C₆alkyloxy,C₁-C₆alkylthio, aryl, arylC₁-C₆alkyl, hetaryl or hetaralkyl, wherein thealkyl, aryl and hetaryl groups independently are optionally substitutedwith one or more of R⁸; orR² together with R³ are forming a saturated or partially saturatedcyclic ring system containing from 3 to 6 carbon atoms and from 0 to 2additional heteroatoms selected from nitrogen, oxygen or sulphur, thering system optionally being substituted with at least one ofC₁-C₆alkyl, aryl, hetaryl, arylC₁-C₆alkyl, hetarylC₁-C₆alkyl, hydroxy,oxo, C₁-C₆alkyloxy, aryloxy, arylC₁-C₆alkyloxy or hetarylC₁-C₆alkyloxy;orR³ together with R⁴ are forming a saturated or partially saturatedcyclic ring system containing from 3 to 6 carbon atoms and from 0 to 2additional heteroatoms selected from nitrogen, oxygen or sulphur, thering system optionally being substituted with at least one ofC₁-C₆alkyl, aryl, hetaryl, arylC₁-C₆alkyl, hetarylC₁-C₆alkyl, hydroxy,oxo, C₁-C₆alkyloxy, aryloxy, arylC₁-C₆alkyloxy or hetarylC₁-C₆alkyloxy;orR⁴ together with R⁵ are forming a saturated or partially saturatedcyclic ring system containing from 3 to 6 carbon atoms and from 0 to 2additional heteroatoms selected from nitrogen, oxygen or sulphur, thering system optionally being substituted with at least one ofC₁-C₆alkyl, aryl, hetaryl, arylC₁-C₆alkyl, hetarylC₁-C₆alkyl, hydroxy,oxo, C₁-C₆alkyloxy, aryloxy, arylC₁-C₆alkyloxy or hetarylC₁-C₆alkyloxy;R⁶ is aryl, hetaryl, arylC₁-C₆alkyl, C₃-C₁₀cycloalkyl,C₃-C₁₀hetcycloalkyl, C₃-C₁₀cycloalkylC₁-C₆alkyl,C₁-C₆alkylcarboxyC₁-C₆alkyl, wherein the alkyl, aryl and cycloalkylgroups independently are optionally substituted with one or more of R¹¹;R⁷ is C₁-C₈alkyl, aryl, hetaryl, arylC₁-C₆alkyl, C₃-C₁₀cycloalkyl,C₃-C₁₀hetcycloalkyl, C₃-C₁₀cycloalkylC₁-C₆alkyl,C₁-C₆alkylcarboxyC₁-C₆alkyl, wherein the alkyl, aryl and cycloalkylgroups independently are optionally substituted with one or more of R¹¹;orR⁶ and R⁷, together with the nitrogen to which they are attached, areforming a saturated or partially saturated cyclic, bicyclic or tricyclicring system containing from 6 to 10 carbon atoms and from 0 to 2additional heteroatoms selected from nitrogen, oxygen or sulphur, thering system optionally being substituted with at least one ofC₁-C₈alkyl, aryl, hetaryl, arylC₁-C₆alkyl, hetarylC₁-C₆alkyl, hydroxy,oxo, cyano, C₁-C₆alkyloxy, arylC₁-C₆alkyloxy, hetarylC₁-C₆alkyloxy,C₁-C₆alkyloxyC₁-C₆alkyl, C₁-C₆alkylcarbonyl, arylcarbonyl,hetarylcarbonyl, arylC₁-C₆alkylcarbonyl, hetarylC₁-C₆alkylcarbonyl,C₁-C₆alkylcarboxy, arylcarboxy or arylC₁-C₆-alkylcarboxy wherein thealkyl and aryl groups independently are optionally substituted with oneor more of R⁸;R⁹ and R¹⁰ independently are hydrogen, C₁-C₈alkyl, aryl, hetaryl,arylC₁-C₆alkyl, C₃-C₁₀-cycloalkyl, C₃-C₁₀hetcycloalkyl,C₃-C₁₀cycloalkylC₁-C₆alkyl, C₁-C₆alkylcarboxyC₁-C₆alkyl, wherein thealkyl, aryl and cycloalkyl groups independently are optionallysubstituted with one or more of R¹¹; orR⁹ and R¹⁰, together with the nitrogen to which they are attached, areforming a saturated or partially saturated cyclic, bicyclic or tricyclicring system containing from 4 to 10 carbon atoms and from 0 to 2additional heteroatoms selected from nitrogen, oxygen or sulphur, thering system optionally being substituted with at least one ofC₁-C₈alkyl, aryl, hetaryl, arylC₁-C₆alkyl, hetarylC₁-C₆alkyl, hydroxy,oxo, cyano, C₁-C₆alkyloxy, arylC₁-C₆alkyloxy, hetarylC₁-C₆alkyloxy,C₁-C₆alkyloxyC₁-C₆alkyl, C₁-C₆alkylcarbonyl, arylcarbonyl,hetarylcarbonyl, arylC₁-C₆alkylcarbonyl, hetarylC₁-C₆alkylcarbonyl,C₁-C₆alkylcarboxy, arylcarboxy or arylC₁-C₆-alkylcarboxy wherein thealkyl and aryl groups independently are optionally substituted with oneor more of R⁸;R⁸ and R¹¹ independently are hydrogen, halo, hydroxy, oxo, nitro, cyano,C₁-C₈alkyl, C₁-C₆-alkyloxy or aryloxy; ora salt thereof with a pharmaceutically acceptable acid or base, or anyoptical isomer or mixture of optical isomers, including a racemicmixture, or any tautomeric forms.

In one embodiment of the present invention, in formula (IV) R¹ ishydrogen or C₁-C₆alkyl, wherein the alkyl group is optionallysubstituted with one or more of R⁸.

In another embodiment of the present invention, in formula (IV) R¹ ishydrogen.

In another embodiment of the present invention, in formula (IV) R², R³,R⁴ and R⁵ are hydrogen.

In another embodiment of the present invention, in formula (IV) R³together with R⁴ are forming a saturated or partially saturated cyclicring system containing from 3 to 6 carbon atoms and from 0 to 2additional heteroatoms selected from nitrogen or oxygen, the ring systemoptionally being substituted with at least one of C₁-C₆alkyl, aryl,hetaryl, arylC₁-C₆alkyl, hetarylC₁-C₆alkyl, hydroxy, oxo, C₁-C₆alkyloxy,aryloxy, arylC₁-C₆alkyloxy or hetarylC₁-C₆alkyloxy.

In another embodiment of the present invention, in formula (IV) R⁴together with R⁵ are forming a saturated or partially saturated cyclicring system containing from 3 to 6 carbon atoms and from 0 to 2additional heteroatoms selected from nitrogen or oxygen, the ring systemoptionally being substituted with at least one of C₁-C₆alkyl, aryl,hetaryl, arylC₁-C₆alkyl, hetarylC₁-C₆alkyl, hydroxy, oxo, C₁-C₆alkyloxy,aryloxy, arylC₁-C₆alkyloxy or hetarylC₁-C₆alkyloxy.

In another embodiment of the present invention, in formula (IV) R⁶ andR⁷, together with the nitrogen to which they are attached, are forming asaturated or partially saturated cyclic, bicyclic or tricyclic ringsystem containing from 6 to 10 carbon atoms and from 0 to 2 additionalheteroatoms selected from nitrogen or oxygen, the ring system optionallybeing substituted with at least one of C₁-C₈alkyl, aryl, hetaryl,arylC₁-C₆alkyl, hetarylC₁-C₆alkyl, hydroxy, oxo, cyano, C₁-C₆alkyloxy,arylC₁-C₆alkyloxy, hetarylC₁-C₆alkyloxy, C₁-C₆alkyloxyC₁-C₆alkyl,C₁-C₆alkylcarbonyl, arylcarbonyl, hetarylcarbonyl,arylC₁-C₆alkylcarbonyl, hetarylC₁-C₆alkylcarbonyl, C₁-C₆alkylcarboxy,arylcarboxy or arylC₁-C₆alkylcarboxy wherein the alkyl and aryl groupsindependently are optionally substituted with one or more of R⁸;

In another embodiment of the present invention, in formula (IV) R⁶ andR⁷; together with the nitrogen to which they are attached, are forming asaturated or partially saturated bicyclic or tricyclic ring systemcontaining from 6 to 10 carbon atoms and from 0 to 2 additionalheteroatoms selected from nitrogen or oxygen, the ring system optionallybeing substituted with at least one of C₁-C₈alkyl, aryl, hetaryl,arylC₁-C₆alkyl, hetarylC₁-C₆alkyl, hydroxy, oxo, cyano, C₁-C₆alkyloxy,arylC₁-C₆alkyloxy, hetarylC₁-C₆alkyloxy, C₁-C₆alkyloxyC₁-C₆alkyl,C₁-C₆-alkylcarbonyl, arylcarbonyl, hetarylcarbonyl,arylC₁-C₆alkylcarbonyl, hetarylC₁-C₆alkylcarbonyl, C₁-C₆alkylcarboxy,arylcarboxy or arylC₁-C₆alkylcarboxy wherein the alkyl and aryl groupsindependently are optionally substituted with one or more of R⁸.

In another embodiment of the present invention, in formula (IV) R⁹ andR¹⁰, together with the nitrogen to which they are attached, are forminga saturated or partially saturated cyclic, bicyclic or tricyclic ringsystem containing from 4 to 10 carbon atoms and from 0 to 2 additionalheteroatoms selected from nitrogen or oxygen, the ring system optionallybeing substituted with at least one of C₁-C₈alkyl, aryl, hetaryl,arylC₁-C₆alkyl, hetarylC₁-C₆alkyl, hydroxy, oxo, cyano, C₁-C₆alkyloxy,arylC₁-C₆alkyloxy, hetarylC₁-C₆alkyloxy, C₁-C₆alkyloxyC₁-C₆alkyl,C₁-C₆alkylcarbonyl, arylcarbonyl, hetarylcarbonyl,arylC₁-C₆alkylcarbonyl, hetarylC₁-C₆alkylcarbonyl, C₁-C₆alkylcarboxy,arylcarboxy or arylC₁-C₆alkylcarboxy wherein the alkyl and aryl groupsindependently are optionally substituted with one or more of R⁸.

In another embodiment of the present invention a compound of the generalformula (IV) or a prodrug thereof ispyrazolo[1,5-a]pyridin-3-yl-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone;or a salt thereof with a pharmaceutically acceptable acid or base, orany optical isomer or mixture of optical isomers, including a racemicmixture, or any tautomeric forms.

In another embodiment of the present invention the compounds of thegeneral formula (IV) or a prodrug thereof are:

-   (2-Methyl-pyrazolo[1,5-a]pyridin-3-yl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone;-   Pyrazolo[1,5-a]pyridine-3-carboxylic acid cyclohexyl-methyl-amide;    or    a salt thereof with a pharmaceutically acceptable acid or base, or    any optical isomer or mixture of optical isomers, including a    racemic mixture, or any tautomeric forms.

In another embodiment, the present invention is concerned with compoundsor prodrugs thereof of the general formula (V)Accordingly, the present invention is concerned with compounds orprodrugs thereof of the general formula (V):

whereinR¹ is hydrogen, C₁-C₈alkyl, C₁-C₆alkyloxyC₁-C₆alkyl, aryl, hetaryl,arylC₁-C₆alkyl, hetarylC₁-C₆alkyl, C₁-C₆SO₂, arylSO₂, hetarylSO₂,arylC₁-C₆alkylSO₂ or hetarylC₁-C₆alkylSO₂ all of which is optionallysubstituted with one or more R⁸;R² and R⁵ independently are hydrogen, halo, nitro, cyano, trihalomethyl,C₁-C₆alkyl, aryl, arylC₁-C₆alkyl, hetaryl or hetarylC₁-C₆alkyl whereinthe alkyl, aryl, arylalkyl, hetaryl and hetarylalkyl groupsindependently are substituted with one or more R⁹; and either R³ ishydrogen; and R⁴ is C(O)NR⁷R⁸; or R³ is C(O)NR⁷R⁸; and R⁴ is hydrogen;andR⁶ is hydrogen, halo, cyano, trihalomethyl, NR¹²R¹³, C₁-C₆alkyl, aryl,arylC₁-C₆alkyl, hetaryl or hetarylC₁-C₆alkyl wherein the alkyl, aryl,arylalkyl, hetaryl and hetarylalkyl groups independently are substitutedwith one or more R⁹; andR⁷ and R⁸ independently are C₁-C₈alkyl, C₃-C₁₀cycloalkyl,C₃-C₁₀hetcycloalkyl, C₃-C₁₀cycloalkylC₁-C₆alkyl, wherein the alkyl,cycloalkyl and hetcycloalkyl groups independently are optionallysubstituted with one or more of R¹⁰; orR⁷ and R⁸ together with the nitrogen to which they are attached, areforming a saturated or partially saturated bicyclic or tricyclic ringsystem containing from 6 to 10 carbon atoms and from 0 to 2 additionalheteroatoms selected from nitrogen or oxygen, the ring system optionallybeing substituted with at least one of C₁-C₈alkyl, arylC₁-C₆alkyl,hetarylC₁-C₆alkyl, hydroxy, cyano, C₁-C₆alkyloxy, arylC₁-C₆alkyloxy,hetarylC₁-C₆alkyloxy, C₁-C₆alkyloxyC₁-C₆alkyl, C₁-C₆alkylcarbonyl,arylcarbonyl, hetarylcarbonyl, arylC₁-C₆alkylcarbonyl,hetarylC₁-C₆alkylcarbonyl, C₁-C₆alkylcarboxy, arylcarboxy orarylC₁-C₆alkylcarboxy wherein the alkyl and aryl groups independentlyare optionally substituted with one or more of R¹¹;R⁹ is hydrogen, hydroxy, oxo, halo, nitro, cyano, C₁-C₆alkyl,C₁-C₆alkyloxy, trihalomethyl, trihalomethoxy, NR¹²R¹³, C(O)NR¹²R¹³,arylC₁-C₆alkyloxy, C₁-C₆alkylcarbonyl, arylcarbonyl,arylC₁-C₆alkylcarbonyl, C₁-C₆alkylcarboxy, arylcarboxy orarylC₁-C₆alkylcarboxy;R¹⁰ and R¹¹ independently are hydrogen, halo, oxo, hydroxy, C₁-C₆alkyl,aryl, arylC₁-C₆alkyl, hetaryl or hetarylalkyl;R¹² and R¹³ independently are hydrogen, C₁-C₈alkyl, aryl, hetaryl,arylC₁-C₆alkyl, C₃-C₁₀-cycloalkyl, C₃-C₁₀hetcycloalkyl,C₃-C₁₀cycloalkylC₁-C₆alkyl, C₁-C₆alkylcarbonyl, arylcarbonyl,arylC₁-C₈alkylcarbonyl, hetarylcarbonyl, hetarylC₁-C₆alkylcarbonyl,C₁-C₆alkylcarboxyC₁-C₆alkyl; orR¹² and R¹³ together with the nitrogen to which they are attached, areforming a saturated or partially saturated cyclic, bicyclic or tricyclicring system containing from 4 to 10 carbon atoms and from 0 to 2additional heteroatoms selected from nitrogen, oxygen or sulphur, thering system optionally being substituted with at least one ofC₁-C₈alkyl, aryl, hetaryl, arylC₁-C₆alkyl, hetarylC₁-C₆alkyl, hydroxy,oxo, cyano, C₁-C₆alkyloxy, arylC₁-C₆alkyloxy, hetarylC₁-C₆alkyloxy,C₁-C₆alkyl-oxyC₁-C₆alkyl, C₁-C₆alkylcarbonyl, arylcarbonyl,hetarylcarbonyl, arylC₁-C₆alkyl-carbonyl, hetarylC₁-C₆alkylcarbonyl,C₁-C₆alkylcarboxy, arylcarboxy or arylC₁-C₆alkylcarboxy; ora salt thereof with a pharmaceutically acceptable acid or base, or anyoptical isomer or mixture of optical isomers, including a racemicmixture, a prodrug thereof, or any tautomeric forms.

In another embodiment, the present invention is concerned with compoundsor prodrugs thereof of the general formula (Va)

whereinR¹ is hydrogen, C₁-C₈alkyl, aryl, hetaryl, arylC₁-C₆alkyl orhetarylC₁-C₆alkyl optionally substituted with one or more R⁸;R² and R⁵ independently are hydrogen, halo, nitro, cyano, trihalomethyl,C₁-C₆alkyl, aryl, arylC₁-C₆alkyl, hetaryl or hetarylC₁-C₆alkyl whereinthe alkyl, aryl, arylalkyl, hetaryl and hetarylalkyl groupsindependently are substituted with one or more R⁸; andeither R³ is hydrogen; and R⁴ is C(O)NR⁶R⁷; or R³ is C(O)NR⁶R⁷; and R⁴is hydrogen;R⁶ and R⁷ independently are C₁-C₈alkyl, C₃-C₁₀cycloalkyl,C₃-C₁₀hetcycloalkyl, C₃-C₁₀cycloalkylC₁-C₆alkyl, wherein the alkyl,cycloalkyl and hetcycloalkyl groups independently are optionallysubstituted with one or more of R⁹; orR⁶ and R⁷ together with the nitrogen to which they are attached, areforming a saturated or partially saturated bicyclic or tricyclic ringsystem containing from 6 to 10 carbon atoms and from 0 to 2 additionalheteroatoms selected from nitrogen or oxygen, the ring system optionallybeing substituted with at least one of C₁-C₈alkyl, arylC₁-C₆alkyl,hetarylC₁-C₆alkyl, hydroxy, cyano, C₁-C₆alkyloxy, arylC₁-C₆alkyloxy,hetarylC₁-C₆alkyloxy, C₁-C₆alkyloxyC₁-C₆alkyl, C₁-C₆alkylcarbonyl,arylcarbonyl, hetarylcarbonyl, arylC₁-C₆alkylcarbonyl,hetarylC₁-C₆alkylcarbonyl, C₁-C₆alkylcarboxy, arylcarboxy orarylC₁-C₆alkylcarboxy wherein the alkyl and aryl groups independentlyare optionally substituted with one or more of R¹⁰;R⁸ is hydrogen, hydroxy, oxo, halo, nitro, cyano, C₁-C₆alkyl,C₁-C₆alkyloxy, trihalomethyl, trihalomethoxy, NR¹¹R¹²,arylC₁-C₆alkyloxy, C₁-C₆alkylcarbonyl, arylcarbonyl,arylC₁-C₆alkylcarbonyl,C₁-C₆alkylcarboxy, arylcarboxy or arylC₁-C₆alkylcarboxy;R⁹ and R¹⁰ independently are hydrogen, halo, oxo, hydroxy, C₁-C₆alkyl,aryl, arylC₁-C₆alkyl, hetaryl or hetarylalkyl;R¹¹ and R¹² independently are hydrogen, C₁-C₈alkyl, aryl, hetaryl,arylC₁-C₆alkyl, C₃-C₁₀-cycloalkyl, C₃-C₁₀hetcycloalkyl,C₃-C₁₀cycloalkylC₁-C₆alkyl, C₁-C₆alkyl-carboxyC₁-C₆alkyl; orR¹¹ and R¹² together with the nitrogen to which they are attached, areforming a saturated or partially saturated cyclic, bicyclic or tricyclicring system containing from 4 to 10 carbon atoms and from 0 to 2additional heteroatoms selected from nitrogen, oxygen or sulphur, thering system optionally being substituted with at least one ofC₁-C₈alkyl, aryl, hetaryl, arylC₁-C₆alkyl, hetarylC₁-C₆alkyl, hydroxy,oxo, cyano, C₁-C₆alkyloxy, arylC₁-C₆alkyloxy, hetarylC₁-C₆alkyloxy,C₁-C₆alkyl-oxyC₁-C₆alkyl, C₁-C₆alkylcarbonyl, arylcarbonyl,hetarylcarbonyl, arylC₁-C₆alkyl-carbonyl, hetarylC₁-C₆alkylcarbonyl,C₁-C₆alkylcarboxy, arylcarboxy or arylC₁-C₆alkylcarboxy; ora salt thereof with a pharmaceutically acceptable acid or base, or anyoptical isomer or mixture of optical isomers, including a racemicmixture, or any tautomeric forms.

In another embodiment of the present invention, in formula (V) and (Va)R¹ is hydrogen, C₁-C₈alkyl, arylC₁-C₆alkyl, hetarylC₁-C₆alkyl, arylSO₂,hetarylSO₂, arylC₁-C₆alkylSO₂ or hetarylC₁-C₆alkylSO₂ all of which isoptionally substituted with one or more R⁸.

In another embodiment of the present invention, in formula (V) and (Va)R¹ is hydrogen, C₁-C₈alkyl, arylC₁-C₆alkyl, hetarylC₁-C₆alkyl all ofwhich is optionally substituted with one or more R⁸.

In another embodiment of the present invention, in formula (V) and (Va)R¹ is arylSO₂, hetarylSO₂, arylC₁-C₆alkylSO₂ or hetarylC₁-C₆alkylSO₂ allof which is optionally substituted with one or more R⁸.

In another embodiment of the present invention, in formula (V) and (Va)R² is hydrogen.

In another embodiment of the present invention, in formula (V) and (Va)R³ is hydrogen and R⁴ is C(O)NR⁷R⁸.

In another embodiment of the present invention, in formula (V) and (Va)R³ is C(O)NR⁷R⁸ and R⁴ is hydrogen.

In another embodiment of the present invention, in formula (V) and (Va)R⁵ is hydrogen.

In another embodiment of the present invention, in formula (V) R⁶ ishydrogen, NR¹²R¹³, C₁-C₆alkyl, aryl or hetaryl wherein the alkyl, aryland hetaryl independently are substituted with one or more R⁹.

In another embodiment of the present invention, in formula (V) and (Va)R⁷ and R⁸ independently are C₁-C₈alkyl or C₃-C₁₀cycloalkyl, wherein thealkyl and cycloalkyl groups independently are optionally substitutedwith one or more of R¹⁰.

In another embodiment of the present invention, in formula (V) and (Va)R⁷ and R⁸ together with the nitrogen to which they are attached, areforming a saturated or partially saturated bicyclic or tricyclic ringsystem containing from 6 to 10 carbon atoms and from 0 to 2 additionalheteroatoms selected from nitrogen or oxygen, the ring system optionallybeing substituted with at least one of C₁-C₈alkyl, arylC₁-C₆alkyl,hetarylC₁-C₆alkyl, hydroxy, cyano, C₁-C₆alkyloxy, arylC₁-C₆alkyloxy,hetarylC₁-C₆alkyloxy, C₁-C₆alkyloxyC₁-C₆alkyl, C₁-C₆alkylcarbonyl,arylcarbonyl, hetarylcarbonyl, arylC₁-C₆alkylcarbonyl,hetarylC₁-C₆alkylcarbonyl, C₁-C₆alkylcarboxy, arylcarboxy orarylC₁-C₆alkylcarboxy wherein the alkyl and aryl groups independentlyare optionally substituted with one or more of R¹¹.

In another embodiment of the present invention, in formula (V) and (Va)R⁹ is hydrogen, hydroxy, oxo, halo, nitro, cyano, C₁-C₆alkyl,C₁-C₆alkyloxy, trihalomethyl, trihalomethoxy, NR¹²R¹³, C(O)NR¹²R¹³,arylC₁-C₆alkyloxy, C₁-C₆alkylcarbonyl, arylcarbonyl,arylC₁-C₆alkylcarbonyl.

In another embodiment of the present invention, in formula (V) and (Va)R¹⁰ and R¹¹ independently are hydrogen, halo, oxo, hydroxy, C₁-C₆alkyl,aryl, arylC₁-C₆alkyl, hetaryl or hetarylalkyl.

In another embodiment of the present invention, in formula (V) and (Va)R¹¹ and R¹² together with the nitrogen to which they are attached, areforming a saturated or partially saturated cyclic, bicyclic or tricyclicring system containing from 4 to 10 carbon atoms and from 0 to 2additional heteroatoms selected from nitrogen or oxygen, the ring systemoptionally being substituted with at least one of C₁-C₈alkyl, aryl,hetaryl, arylC₁-C₆alkyl, hetarylC₁-C₆alkyl, hydroxy, oxo, cyano,C₁-C₆alkyloxy, arylC₁-C₆alkyloxy, hetarylC₁-C₆alkyloxy,C₁-C₆alkyl-oxyC₁-C₆alkyl, C₁-C₆alkylcarbonyl, arylcarbonyl,hetarylcarbonyl, arylC₁-C₆alkyl-carbonyl, hetarylC₁-C₆alkylarbonyl,C₁-C₆alkylcarboxy, arylcarboxy or arylC₁-C₆alkylcarboxy.

In another embodiment of the present invention the compound of thegeneral formulas (V) and (Va), or a prodrug thereof is1H-Benzoimidazole-5-carboxylic acid cyclohexyl-methyl-amide; or a saltthereof with a pharmaceutically acceptable acid or base, or any opticalisomer or mixture of optical isomers, including a racemic mixture, orany tautomeric forms.

In yet another embodiment of the present invention the compounds of thegeneral formulas (V) and (Va), or a prodrug thereof is selected from thegroup consisting of:

-   1-Benzyl-1H-benzoimidazole-5-carboxylic acid    cyclohexyl-methyl-amide;-   (1H-Benzoimidazol-5-yl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone;    or    a salt thereof with a pharmaceutically acceptable acid or base, or    any optical isomer or mixture of optical isomers, including a    racemic mixture, or any tautomeric forms.

In another embodiment of the present invention, the compounds of generalformulas (V) and (Va), or a prodrug thereof is selected from the groupconsisting of:

-   Isopropyl-2-trifluoromethyl-1H-benzoimidazole-5-carboxylic acid    cyclohexyl-methyl-amide;-   1-Benzyl-1H-benzoimidazole-5-carboxylic acid    cyclohexyl-methyl-amide;-   2-Methyl-1H-benzoimidazole-5-carboxylic acid    cyclohexyl-methyl-amide;-   2-Hydroxymethyl-1H-benzoimidazole-5-carboxylic acid    cyclohexyl-methyl-amide;-   2-(4-Amino-phenyl)-1H-benzoimidazole-5-carboxylic acid    cyclohexyl-methyl-amide;-   (1H-Benzoimidazol-5-yl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone;-   (2-Methyl-1H-benzoimidazol-5-yl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone;-   (2-Amino-1H-benzoimidazol-5-yl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone;-   (2-Benzo[1,3]dioxol-5-yl-1H-benzoimidazol-5-yl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone;-   3-[5-(1,3,3-Trimethyl-6-aza-bicyclo[3.2.1]octane-6-carbonyl)-1H-benzoimidazol-2-yl]-benzoic    acid methyl ester;-   (2-Thiophen-2-yl-1H-benzoimidazol-5-yl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone;-   [2-(2-Nitro-phenyl)-1H-benzoimidazol-5-yl]-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone;    or    a salt thereof with a pharmaceutically acceptable acid or base, or    any optical isomer or mixture of optical isomers, including a    racemic mixture, a prodrug thereof, or any tautomeric forms.

In another embodiment, the present invention is concerned with compoundsor prodrugs thereof of the general formula (VI)

whereinX is oxygen or (CR¹R²)_(n);R¹, R², R³, and R⁴ independently are hydrogen, C₁-C₆alkyl, aryl,arylC₁-C₆alkyl, hetaryl or hetarylC₁-C₆alkyl optionally substituted withone or more R⁸ independently; orR¹ and either R³ or R⁴ together are forming a saturated or partiallysaturated ring system containing from 4 to 8 carbon atoms, the ringsystem optionally being substituted with at least one of C₁-C₆alkyl,hydroxy, oxo, aryl, hetaryl, arylC₁-C₆alkyl or hetarylC₁-C₆alkyl; orR¹ and either R³ or R⁴ together with the single bond are forming acarbon-carbon double bond;R⁵ is C₁-C₈alkyl optionally substituted with one or more of R⁹;R⁶ is C₃-C₁₀cycloalkyl, C₃-C₁₀hetcycloalkyl, C₃-C₁₀cycloalkylC₁-C₆alkyl,wherein the alkyl, cycloalkyl and hetcycloalkyl groups independently areoptionally substituted with one or more of R⁹; orR⁵ and R⁶ together with the nitrogen to which they are attached, areforming a saturated or partially saturated cyclic, bicyclic or tricyclicring system containing from 6 to 10 carbon atoms and from 0 to 2additional heteroatoms selected from nitrogen, oxygen or sulphur, thering system optionally being substituted with at least one ofC₁-C₆alkyl, aryl, hetaryl, arylC₁-C₆alkyl, hetarylC₁-C₆alkyl, hydroxy,oxo, cyano, C₁-C₆alkyloxy, arylC₁-C₆alkyloxy, hetarylC₁-C₆alkyloxy,C₁-C₆alkyloxyC₁-C₆alkyl, C₁-C₆alkylcarbonyl, arylcarbonyl,hetarylcarbonyl, arylC₁-C₆alkylcarbonyl, hetarylC₁-C₆alkylcarbonyl,C₁-C₆alkylcarboxy, arylcarboxy or arylC₁-C₆alkylcarboxy wherein thealkyl and aryl groups independently are optionally substituted with oneor more of R¹⁰;R⁷ is hydrogen, halo, nitro, NR¹²R¹³, cyano, trihalomethyl, C₁-C₆alkyl,aryl, arylC₁-C₆alkyl, C₁-C₆alkyloxy, aryloxy, arylC₁-C₆alkyloxy,hetaryl, hetarylC₁-C₆alkyl, hetaryloxy or hetarylC₁-C₆-alkyloxyoptionally substituted with one or more R¹¹ independently;R⁸ and R⁹ independently are hydrogen, hydroxy, oxo, halo, nitro, cyano,C₁-C₆alkyl, C₁-C₆-alkyloxy, trihalomethyl, trihalomethoxy, NR¹²R¹³,arylC₁-C₆alkyloxy, C₁-C₆alkylcarbonyl, arylcarbonyl,arylC₁-C₆alkylcarbonyl, C₁-C₆alkylcarboxy, arylcarboxy orarylC₁-C₆alkylcarboxy;R¹⁰ is hydrogen, C₁-C₈alkyl, arylC₁-C₆alkyl, hetarylC₁-C₆alkyl,C₁-C₆alkyloxy, arylC₁-C₆alkyloxy, hetarylC₁-C₆alkyloxy;R¹¹ is hydrogen, halo, hydroxy, oxo, nitro, cyano, C₁-C₈alkyl,C₁-C₆alkyloxy, aryloxy or hetaryloxy;R¹² and R¹³ independently are hydrogen, C₁-C₈alkyl, aryl, hetaryl,arylC₁-C₆alkyl, C₃-C₁₀cycloalkyl, C₃-C₁₀hetcycloalkyl,C₁-C₆alkylcarbonyl, arylC₁-C₆alkylcarbonyl, C₃-C₁₀cycloalkylC₁-C₆-alkyl,C₁-C₆alkyloxycarbonyl; orR¹² and R¹³ are together with the nitrogen to which they are attached,are forming a saturated or partially saturated cyclic, bicyclic ortricyclic ring system containing from 4 to 10 carbon atoms and from 0 to2 additional heteroatoms selected from nitrogen, oxygen or sulphur, thering system optionally being substituted with at least one ofC₁-C₆alkyl, aryl, hetaryl, arylC₁-C₆alkyl, hetarylC₁-C₆alkyl, hydroxy,oxo, cyano, C₁-C₆alkyloxy, arylC₁-C₆alkyloxy, hetarylC₁-C₆alkyloxy,C₁-C₆alkyloxyC₁-C₆alkyl, C₁-C₆alkylcarbonyl, arylcarbonyl,hetarylcarbonyl, arylC₁-C₆alkylcarbonyl, hetarylC₁-C₆alkylcarbonyl,C₁-C₆alkylcarboxy, arylcarboxy or arylC₁₋₆alkylcarboxy;

-   n is 1 or 2; or    a salt thereof with a pharmaceutically acceptable acid or base, or    any optical isomer or mixture of optical isomers, including a    racemic mixture, a prodrug thereof, or any tautomeric forms.

In one embodiment of the present invention, in formula (VI) X is(CR¹R²)_(n), wherein R¹, R² and n are as defined above.

In another embodiment of the present invention, in formula (VI) n is 1.

In another embodiment of the present invention, in formula (VI) X isoxygen.

In another embodiment of the present invention, in formula (VI) R¹, R²,R³, and R⁴ independently are hydrogen, C₁-C₆alkyl or arylC₁-C₆alkyl,optionally substituted with one or more R⁸.

In another embodiment of the present invention, in formula (VI) R¹ andeither R³ or R⁴ together with the single bond are forming acarbon-carbon double bond.

In another embodiment of the present invention, in formula (VI) R⁵ isC₁-C₈alkyl optionally substituted with one or more of R⁹.

In another embodiment of the present invention, in formula (VI) R⁶ isC₃-C₁₀cycloalkyl or C₃-C₁₀hetcycloalkyl each of which is optionallysubstituted with one or more of R⁹.

In another embodiment of the present invention, in formula (VI) R⁶ isC₃-C₁₀cycloalkyl optionally substituted with one or more of R⁹.

In another embodiment of the present invention, in formula (VI) R⁵ andR⁶ together with the nitrogen to which they are attached, are forming asaturated or partially saturated cyclic, bicyclic or tricyclic ringsystem containing from 6 to 10 carbon atoms and from 0 to 2 additionalheteroatoms selected from nitrogen, oxygen or sulphur, the ring systemoptionally being substituted with at least one of C₁-C₆alkyl, aryl,hetaryl, arylC₁-C₆alkyl, hetarylC₁-C₆alkyl, hydroxy, oxo, cyano,C₁-C₆alkyloxy, arylC₁-C₆alkyloxy, hetarylC₁-C₆alkyloxy,C₁-C₆alkyloxyC₁-C₆alkyl, C₁-C₆alkylcarbonyl, arylcarbonyl,hetarylcarbonyl, arylC₁-C₆alkylcarbonyl, hetarylC₁-C₆alkylcarbonyl,C₁-C₆alkylcarboxy, arylcarboxy or arylC₁-C₆alkylcarboxy wherein thealkyl and aryl groups independently are optionally substituted with oneor more of R¹⁰.

In another embodiment of the present invention, in formula (VI) R⁷ ishydrogen, halo, NR¹²R¹³, trihalomethyl, C₁-C₆alkyloxy, aryloxy,arylC₁-C₆alkyloxy or hetaryloxy optionally substituted with one or moreR¹¹ independently.

In another embodiment of the present invention, in formula (VI) R⁸ andR⁹ independently are hydrogen, hydroxy, oxo, halo, nitro, cyano,C₁-C₆alkyl, C₁-C₆alkyloxy, trihalomethyl, or NR¹²R¹³.

In another embodiment of the present invention, in formula (VI) R¹⁰ ishydrogen or C₁-C₈alkyl.

In yet another embodiment of the present invention, in formula (VI) thebicyclic ring system is 6-aza-bicyclo[3.2.1]octane optionallysubstituted with one or more of C₁-C₆alkyl.

In yet another embodiment of the present invention, in formula (VI) thebicyclic ring system is 1,3,3-trimethyl-6-aza-bicyclo[3.2.1]octane.

In yet another embodiment of the present invention a compound of thegeneral formula (VI) or a prodrug thereof is2,3-Dimethyl-2,3-dihydro-benzofuran-7-carboxylic acidcyclohexylmethyl-amide or a salt thereof with a pharmaceuticallyacceptable acid or base, or any optical isomer or mixture of opticalisomers, including a racemic mixture, or any tautomeric forms.

In another embodiment of the present invention the compounds of thegeneral formula (VI) or a prodrug thereof is selected from the groupconsisting of:

-   2,5-Dimethyl-3-phenyl-benzofuran-7-carboxylic acid    cyclohexyl-methyl-amide;-   2,2-Dimethyl-2,3-dihydro-benzofuran-7-carboxylic acid    cyclohexyl-methyl-amide;-   2-Methyl-2,3-dihydro-benzofuran-7-carboxylic acid    cyclohexyl-methyl-amide;-   (2,3-Dimethyl-2,3-dihydro-benzofuran-7-yl)-(2,4,4-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone;-   4-Methoxy-2-methyl-2,3-dihydro-benzofuran-7-carboxylic acid    cyclohexyl-methyl-amide;-   2-Methyl-benzofuran-7-carboxylic acid cyclohexyl-methyl-amide;-   (2-Methyl-2,3-dihydro-benzofuran-7-yl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone;-   Benzofuran-7-carboxylic acid cyclohexyl-methyl-amide;-   2,3-Dihydro-benzofuran-7-carboxylic acid cyclohexyl-methyl-amide;-   3,3-Dimethyl-2,3-dihydro-benzofuran-7-carboxylic acid    cyclohexyl-methyl-amide;-   Chroman-8-carboxylic acid cyclohexyl-methyl-amide; or    a salt thereof with a pharmaceutically acceptable acid or base, or    any optical isomer or mixture of optical isomers, including a    racemic mixture, or any tautomeric forms.

In another embodiment of the present invention the compounds of thegeneral formula (VI) or a prodrug thereof is selected from the groupconsisting of:

-   2,3-Dihydro-benzofuran-7-carboxylic acid cyclohexyl-methyl-amide;-   Benzofuran-7-carboxylic acid cyclohexyl-methyl-amide;-   2-Methyl-2,3-dihydro-benzofuran-7-carboxylic acid    cyclohexyl-methyl-amide;-   2-Methyl-benzofuran-7-carboxylic acid cyclohexyl-methyl-amide;-   3,3-Dimethyl-2,3-dihydro-benzofuran-7-carboxylic acid    cyclohexyl-methyl-amide;-   (2,3-Dimethyl-2,3-dihydro-benzofuran-7-yl)-(2,4,4-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone;-   4-Methoxy-2-methyl-2,3-dihydro-benzofuran-7-carboxylic acid    cyclohexyl-methyl-amide;-   2,2-Dimethyl-2,3-dihydro-benzofuran-7-carboxylic acid    cyclohexyl-methyl-amide;-   (2-Methyl-2,3-dihydro-benzofuran-7-yl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone;-   Chroman-8-carboxylic acid cyclohexyl-methyl-amide; or    a salt thereof with a pharmaceutically acceptable acid or base, or    any optical isomer or mixture of optical isomers, including a    racemic mixture, a prodrug thereof, or any tautomeric forms.

In another embodiment, the present invention is concerned with compoundsor prodrugs thereof of the general formula (VII)

whereinR¹ is hydrogen, C₁-C₈alkyl, hetaryl, arylC₁-C₆alkyl or hetarylC₁-C₆alkyloptionally substituted with one or more R⁹;R², R³, R⁴, R⁵ and R⁶ independently are hydrogen, halo, nitro, cyano,trihalomethyl, carboxy, N(R¹²R¹³), C(O)NR⁷R⁸, C₁-C₈alkyl,C₃-C₁₀cycloalkyl, C₃-C₁₀hetcycloalkyl, N(R¹²R¹³)C₁-C₆alkyl,C₁-C₆alkyloxy, C₁-C₆alkyloxyC₁-C₆alkyl, aryl, arylC₁-C₆alkyl, aryloxy,aryloxyC₁-C₆alkyl, arylC₁-C₆alkyloxy, arylC₁-C₆alkyloxyC₁-C₆alkyl,C₁-C₆alkylcarboxy, arylcarboxy, arylC₁-C₆alkylcarboxy, hetaryl,hetarylC₁-C₆alkyl, hetarylC₁-C₆alkyloxy, hetaryloxyC₁-C₆alkyl orhetarylC₁-C₆alkyloxyC₁-C₆alkyl wherein the alkyl, aryl, arylalkyl,hetaryl and hetarylalkyl groups independently are substituted with oneor more R⁹;R⁷ is hydrogen or C₁-C₈alkyl optionally substituted with one or more ofR¹⁰;R⁸ is C₃-C₁₀cycloalkyl, C₃-C₁₀hetcycloalkyl, C₃-C₁₀cycloalkylC₁-C₆alkyl,wherein the cycloalkyl and hetcycloalkyl groups independently areoptionally substituted with one or more of R¹⁰; orR⁷ and R⁸ together with the nitrogen to which they are attached, areforming a saturated or partially saturated cyclic, bicyclic or tricyclicring system containing from 4 to 10 carbon atoms and from 0 to 2additional heteroatoms selected from nitrogen or oxygen, the ring systemoptionally being substituted with at least one of C₁-C₈alkyl, aryl,hetaryl, arylC₁-C₆alkyl, hetarylC₁-C₆alkyl, hydroxy, oxo, cyano,C₁-C₆alkyloxy, arylC₁-C₆alkyloxy, hetarylC₁-C₆alkyl-oxy,C₁-C₆alkyloxyC₁-C₆alkyl, C₁-C₆alkylcarbonyl, arylcarbonyl,hetarylcarbonyl, arylC₁-C₆alkylcarbonyl, hetarylC₁-C₆alkylcarbonyl,C₁-C₆alkylcarboxy, arylcarboxy or arylC₁-C₆alkylcarboxy wherein thealkyl and aryl groups independently are optionally substituted with oneor more of R¹¹;R⁹ is hydrogen, hydroxy, oxo, halo, nitro, cyano, C₁-C₆alkyl,C₁-C₆alkyloxy, trihalomethyl, trihalomethoxy, NR¹²R¹³,arylC₁-C₆alkyloxy, C₁-C₆alkylcarbonyl, arylcarbonyl,arylC₁-C₆alkylcarbonyl, C₁-C₆alkylcarboxy, arylcarboxy orarylC₁-C₆alkylcarboxy;R¹⁰ and R¹¹ independently are hydrogen, halo, oxo, hydroxy, C₁-C₆alkyl,aryl, arylC₁-C₆alkyl, hetaryl or hetarylalkyl;R¹² and R¹³ independently are hydrogen, C₁-C₈alkyl, aryl, hetaryl,arylC₁-C₆alkyl, C₃-C₁₀-cycloalkyl, C₃-C₁₀hetcycloalkyl,C₃-C₁₀cycloalkylC₁-C₆alkyl, C₁-C₆alkylcarbonyl, arylcarbonyl,arylC₁-C₆alkylcarbonyl, C₃-C₁₀cycloalkylcarbonyl,C₃-C₁₀hetcycloalkylcarbonyl or C₃-C₁₀cycloalkylC₁-C₆alkylcarbonylwherein the alkyl and aryl groups independently are optionallysubstituted with one or more of R¹¹, wherein R¹¹ is as defined above; orR¹² and R¹³ together with the nitrogen to which they are attached, areforming a saturated or partially saturated cyclic, bicyclic or tricyclicring system containing from 4 to 10 carbon atoms and from 0 to 2additional heteroatoms selected from nitrogen, oxygen or sulphur, thering system optionally being substituted with at least one ofC₁-C₈alkyl, aryl, hetaryl, arylC₁-C₆alkyl, hetarylC₁-C₆alkyl, hydroxy,oxo, cyano, C₁-C₆alkyloxy, arylC₁-C₆alkyloxy, hetarylC₁-C₆alkyloxy,C₁-C₆alkyl-oxyC₁-C₆alkyl, C₁-C₆alkylcarbonyl, arylcarbonyl,hetarylcarbonyl, arylC₁-C₆alkylcarbonyl, hetarylC₁-C₆alkylcarbonyl,C₁-C₆alkylcarboxy, arylcarboxy or arylC₁-C₆alkylcarboxy; ora salt thereof with a pharmaceutically acceptable acid or base, or anyoptical isomer or mixture of optical isomers, including a racemicmixture, or any tautomeric forms.

In another embodiment, the present invention is concerned with compoundsor prodrugs thereof of the general formula (VII) wherein

R¹ is hydrogen, C₁-C₈alkyl, hetaryl, arylC₁-C₆alkyl or hetarylC₁-C₆alkyloptionally substituted with one or more R⁹;

R² and R⁵ independently are hydrogen, halo, nitro, cyano, trihalomethyl,C₁-C₆alkyl, C₁-C₆-alkyloxy, C₁-C₆alkyloxyC₁-C₆alkyl, aryl,arylC₁-C₆alkyl, aryloxy, aryloxyC₁-C₆alkyl, arylC₁-C₆-alkyloxy,arylC₁-C₆alkyloxyC₁-C₆alkyl, hetaryl or hetarylC₁-C₆alkyl wherein thealkyl, aryl, arylalkyl, hetaryl and hetarylalkyl groups independentlyare substituted with one or more R⁹; and

either R³ is C(O)NR⁷R⁸, and R⁴ is hydrogen; or R³ is hydrogen, and R⁴ isC(O)NR⁷R⁸;

R⁶ is C₁-C₈alkyl, C₃-C₁₀cycloalkyl, C₃-C₁₀hetcycloalkyl,N(R¹²R¹³)C₁-C₆alkyl, C₁-C₆alkyloxyC₁-C₆-alkyl, aryloxyC₁-C₆alkyl,arylC₁-C₆alkyloxy or arylC₁-C₆alkyloxyC₁-C₆alkyl;

R⁷ is C₁-C₈alkyl optionally substituted with one or more of R¹⁰;

R⁸ is C₃-C₁₀cycloalkyl, C₃-C₁₀hetcycloalkyl, C₃-C₁₀cycloalkylC₁-C₆alkyl,wherein the cycloalkyl and hetcycloalkyl groups independently areoptionally substituted with one or more of R¹⁰; or

R⁷ and R⁸ together with the nitrogen to which they are attached, areforming a saturated or partially saturated cyclic, bicyclic or tricyclicring system containing from 6 to 10 carbon atoms and from 0 to 2additional heteroatoms selected from nitrogen or oxygen, the ring systemoptionally being substituted with at least one of C₁-C₈alkyl, aryl,hetaryl, arylC₁-C₆alkyl, hetarylC₁-C₆alkyl, hydroxy, oxo, cyano,C₁-C₆alkyloxy, arylC₁-C₆alkyloxy, hetarylC₁-C₆alkyl-oxy,C₁-C₆alkyloxyC₁-C₆alkyl, C₁-C₆alkylcarbonyl, arylcarbonyl,hetarylcarbonyl, arylC₁-C₆alkylcarbonyl, hetarylC₁-C₆alkylcarbonyl,C₁-C₆alkylcarboxy, arylcarboxy or arylC₁-C₆alkylcarboxy wherein thealkyl and aryl groups independently are optionally substituted with oneor more of R¹¹;

R⁹ is hydrogen, hydroxy, oxo, halo, nitro, cyano, C₁-C₆alkyl,C₁-C₆alkyloxy, trihalomethyl, trihalomethoxy, NR¹²R¹³,arylC₁-C₆alkyloxy, C₁-C₆alkylcarbonyl, arylcarbonyl,arylC₁-C₆alkylcarbonyl, C₁-C₆alkylcarboxy, arylcarboxy orarylC₁-C₆alkylcarboxy;

R¹⁰ and R¹¹ independently are hydrogen, halo, oxo, hydroxy, C₁-C₆alkyl,aryl, arylC₁-C₆alkyl, hetaryl or hetarylalkyl;

R¹² and R¹³ independently are hydrogen, C₁-C₈alkyl, aryl, hetaryl,arylC₁-C₆alkyl, C₃-C₁₀-cycloalkyl, C₃-C₁₀hetcycloalkyl,C₃-C₁₀cycloalkylC₁-C₆alkyl, C₁-C₆alkylcarbonyl, arylcarbonyl,arylC₁-C₆alkylcarbonyl, C₃-C₁₀cycloalkylcarbonyl,C₃-C₁₀hetcycloalkylcarbonyl or C₃-C₁₀cycloalkylC₁-C₆alkylcarbonyl; or

R¹² and R¹³ together with the nitrogen to which they are attached, areforming a saturated or partially saturated cyclic, bicyclic or tricyclicring system containing from 4 to 10 carbon atoms and from 0 to 2additional heteroatoms selected from nitrogen, oxygen or sulphur, thering system optionally being substituted with at least one ofC₁-C₈alkyl, aryl, hetaryl, arylC₁-C₆alkyl, hetarylC₁-C₆alkyl, hydroxy,oxo, cyano, C₁-C₆alkyloxy, arylC₁-C₆alkyloxy, hetarylC₁-C₆alkyloxy,C₁-C₆alkyl-oxyC₁-C₆alkyl, C₁-C₆alkylcarbonyl, arylcarbonyl,hetarylcarbonyl, arylC₁-C₆alkylcarbonyl, hetarylC₁-C₆alkylcarbonyl,C₁-C₆alkylcarboxy, arylcarboxy or arylC₁-C₆alkylcarboxy; or

a salt thereof with a pharmaceutically acceptable acid or base, or anyoptical isomer or mixture of optical isomers, including a racemicmixture, or any tautomeric forms.

In another embodiment, the present invention, in formula (VII) R² isC(O)NR⁷R⁸ and R³ R⁴ and R⁵ are hydrogen, wherein R⁷ and R⁸ are asdefined above.

In another embodiment, the present invention, in formula (VII) R³ isC(O)NR⁷R⁸ and R² R⁴ and R⁵ are hydrogen, wherein R⁷ and R⁸ are asdefined above.

In another embodiment, the present invention, in formula (VII) R⁴ isC(O)NR⁷R⁸ and R² R³ and R⁵ are hydrogen, wherein R⁷ and R⁸ are asdefined above.

In another embodiment, the present invention, in formula (VII) R⁵ isC(O)NR⁷R⁸ and R² R³ and R⁴ are hydrogen, wherein R⁷ and R⁸ are asdefined above.

In another embodiment, the present invention, in formula (VII) R⁶ isC(O)NR⁷R⁸, wherein R⁷ and R⁸ are as defined above.

In another embodiment, the present invention, in formula (VII) R³ isC(O)NR⁷R⁸ and R⁴ is hydrogen, wherein R⁷ and R⁸ are as defined above.

In another embodiment, the present invention, in formula (VII) R³ ishydrogen and R⁴ is C(O)NR⁷R⁸, wherein R⁷ and R⁸ are as defined above.

In another embodiment, the present invention, in formula (VII) R⁸ isC₃-C₁₀cycloalkyl or C₃-C₁₀hetcycloalkyl, each of which is optionallysubstituted with one or more of R¹⁰, wherein R¹⁰ is as defined above.

In another embodiment, the present invention, in formula (VII) R⁷ and R⁸together with the nitrogen to which they are attached, are forming asaturated or partially saturated bicyclic or tricyclic ring systemcontaining from 6 to 10 carbon atoms and from 0 to 2 additionalheteroatoms selected from nitrogen or oxygen, the ring system optionallybeing substituted with at least one of C₁-C₈alkyl, aryl, hetaryl,arylC₁-C₆alkyl, hetarylC₁-C₆alkyl, hydroxy, oxo, cyano, C₁-C₆alkyloxy,arylC₁-C₆alkyloxy, hetarylC₁-C₆alkyl-oxy, C₁-C₆alkyloxyC₁-C₆alkyl,C₁-C₆alkylcarbonyl, arylcarbonyl, hetarylcarbonyl,arylC₁-C₆alkylcarbonyl, hetarylC₁-C₆alkylcarbonyl, C₁-C₆alkylcarboxy,arylcarboxy or arylC₁-C₆alkylcarboxy wherein the alkyl and aryl groupsindependently are optionally substituted with one or more of R¹¹,wherein R¹¹ is as defined above.

In a further embodiment of the present invention, in formula (VII) thebicyclic ring system is 6-aza-bicyclo[3.2.1]octane optionallysubstituted with one or more C₁-C₆alkyl.

In yet a further embodiment of the present invention, in formula (VII)the bicyclic ring system is 1,3,3-trimethyl-6-aza-bicyclo[3.2.1]octane.

In another embodiment of the present invention the compounds of thegeneral formula (VII) or a prodrug thereof is selected from the groupconsisting of:

-   (1H-Indol-5-yl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone;-   1H-Indole-6-carboxylic acid cyclohexyl-methyl-amide; or    a salt thereof with a pharmaceutically acceptable acid or base, or    any optical isomer or mixture of optical isomers, including a    racemic mixture, or any tautomeric forms.

In another embodiment of the present invention, the compounds orprodrugs thereof of the general formula (VII) are selected from thegroup consisting of the compounds of examples 3 through 20 as describedunder EXAMPLES, COMPOUNDS OF GENERAL FORMULA (VII).

In another embodiment, the present invention is concerned with compoundsor prodrugs thereof of the general formula (VIII)

whereinX is NR⁴, S or O;R¹ and R² independently are hydrogen, halo, cyano, trihalomethyl,C₁-C₆alkyl or C₁-C₆alkyloxy, wherein the alkyl groups independently areoptionally substituted with one or more of R⁷;R³ is hydrogen, C₁-C₆alkyl, C₃-C₁₀cycloalkyl, C₁-C₆alkyloxy,C₁-C₆alkylthio, aryl, arylC₁-C₆alkyl, hetaryl or hetarylalkyl, whereinthe alkyl, cycloalkyl, aryl, hetaryl and hetarylalkyl groupsindependently are optionally substituted with one or more of R⁷;R⁴ is hydrogen, C₁-C₈alkyl, C₁-C₆alkyloxyC₁-C₆alkyl, aryl, hetaryl,hetarylC₁-C₆alkyl, arylC₁-C₆alkyl, arylC₁-C₆alkyloxyC₁-C₆alkyl,C₃-C₁₀cycloalkyl, C₃-C₁₀hetcycloalkyl, C₃-C₁₀cyclo-alkylC₁-C₆alkyl,C₁-C₆alkylcarboxyC₁-C₆alkyl wherein the alkyl, aryl, hetaryl, cycloalkyland hetcycloalkyl groups independently are optionally substituted withone or more of R⁷;R⁵ is hydrogen, and R⁶ is adamantyl optionally substituted with hydroxy,C₁-C₆alkyloxy, aryl, arylC₁-C₆alkyl, aryloxy, arylC₁-C₆alkyloxy,hetaryl, hetaryloxy or hetarylC₁-C₆alkyloxy wherein the alkyl, aryl andhetaryl groups independently are optionally substituted with one or moreof R⁷; orR⁵ and R⁶ are together with the nitrogen to which they are attached,forming a saturated or partially saturated cyclic, bicyclic or tricyclicring system containing from 6 to 10 carbon atoms and from 0 to 2additional heteroatoms selected from nitrogen, oxygen or sulphur, thering system optionally being substituted with at least one ofC₁-C₆alkyl, aryl, hetaryl, arylC₁-C₆alkyl, hetarylalkyl, hydroxy, oxo,cyano, C₁-C₆alkyloxy, arylC₁-C₆alkyloxy, hetarylC₁-C₆alkyloxy,C₁-C₆alkyloxyC₁-C₆alkyl, C₁-C₆alkylcarbonyl, arylcarbonyl,hetarylcarbonyl, arylC₁-C₆alkylcarbonyl, hetarylC₁-C₆alkylcarbonyl,C₁-C₆alkylcarboxy, arylcarboxy or arylC₁-C₆alkylcarboxy wherein thealkyl and aryl groups independently are optionally substituted with oneor more of R⁷;R⁷ are independently hydrogen, halo, hydroxy, oxo, nitro, NR⁹R¹⁰, cyano,COOR⁸, CONR⁹R¹⁰, C₁-C₈alkyl, C₁-C₆alkyloxy, aryloxy, arylC₁-C₆alkyloxy,hetaryloxy or hetarylC₁-C₆alkyloxy;R⁸ is hydrogen, C₁-C₆alkyl, aryl, arylC₁-C₆alkyl, hetarylalkyl, whereinthe alkyl, aryl and hetarylalkyl groups independently are optionallysubstituted with one or more of R⁷;R⁹ and R¹⁰ independently are hydrogen, C₁-C₈alkyl, C₃-C₁₀cycloalkyl,C₃-C₁₀hetcycloalkyl, C₃-C₁₀cycloalkylC₁-C₆alkyl, wherein the alkyl,cycloalkyl and hetcycloalkyl groups independently are optionallysubstituted with one or more of R⁷; orR⁹ and R¹⁰ together with the nitrogen to which they are attached, areforming a saturated or partially saturated bicyclic or tricyclic ringsystem containing from 4 to 10 carbon atoms and from 0 to 2 additionalheteroatoms selected from nitrogen or oxygen, the ring system optionallybeing substituted with at least one of C₁-C₈alkyl, arylC₁-C₆alkyl,hetarylC₁-C₆alkyl, hydroxy, cyano, C₁-C₆alkyloxy, arylC₁-C₆alkyloxy,hetarylC₁-C₆alkyloxy, C₁-C₆alkyloxyC₁-C₆alkyl, C₁-C₆alkylcarbonyl,arylcarbonyl, hetarylcarbonyl, arylC₁-C₆alkylcarbonyl,hetarylC₁-C₆alkylcarbonyl, C₁-C₆alkylcarboxy, arylcarboxy orarylC₁-C₆alkylcarboxy wherein the alkyl and aryl groups independentlyare optionally substituted with one or more of R¹¹;R¹¹ is hydrogen, halo, oxo, hydroxy, C₁-C₆alkyl, aryl, arylC₁-C₆alkyl,hetaryl or hetarylalkyl;a salt thereof with a pharmaceutically acceptable acid or base, or anyoptical isomer or mixture of optical isomers, including a racemicmixture, or any tautomeric forms.

In the definitions of R⁴, in the above formula (VIII), hetcycloalkylcannot be 7-aza[2,2,1]bicycloheptane.

In another embodiment, the present invention is concerned with compoundsor prodrugs thereof of the above general formula (VIII) wherein

X is NR⁴, S or O;

R¹ and R² independently are hydrogen, halo, cyano, trihalomethyl,C₁-C₆alkyl or C₁-C₆alkyloxy, wherein the alkyl groups independently areoptionally substituted with one or more of R⁷;

R³ is hydrogen, C₁-C₆alkyl, C₃-C₁₀cycloalkyl, C₁-C₆alkyloxy,C₁-C₆alkylthio, aryl, arylC₁-C₆alkyl, hetaryl or hetarylalkyl, whereinthe alkyl, cycloalkyl, aryl, hetaryl and hetarylalkyl groupsindependently are optionally substituted with one or more of R⁷;

R⁴ is hydrogen, C₁-C₈alkyl, C₁-C₆alkyloxyC₁-C₆alkyl, aryl, hetaryl,arylC₁-C₆alkyl, arylC₁-C₆alkyloxyC₁-C₆alkyl, C₃-C₁₀cycloalkyl,C₃-C₁₀hetcycloalkyl, C₃-C₁₀cycloalkylC₁-C₆alkyl,C₁-C₆alkylcarboxyC₁-C₆alkyl wherein the alkyl, aryl, hetaryl, cycloalkyland hetcycloalkyl groups independently are optionally substituted withone or more of R⁷;

R⁵ is hydrogen, and R⁶ is adamantyl optionally substituted with hydroxy,C₁-C₆alkyloxy, aryl, arylC₁-C₆alkyl, aryloxy, arylC₁-C₆alkyloxy,hetaryl, hetaryloxy or hetarylC₁-C₆alkyloxy wherein the alkyl, aryl andhetaryl groups independently are optionally substituted with one or moreof R⁷; or

R⁵ and R⁶ are together with the nitrogen to which they are attached,forming a saturated or partially saturated cyclic, bicyclic or tricyclicring system containing from 5 to 10 carbon atoms and from 0 to 2additional heteroatoms selected from nitrogen, oxygen or sulphur, thering system optionally being substituted with at least one ofC₁-C₆alkyl, aryl, hetaryl, arylC₁-C₆alkyl, hetarylalkyl, hydroxy, oxo,cyano, C₁-C₆alkyloxy, arylC₁-C₆alkyloxy, hetarylC₁-C₆alkyloxy,C₁-C₆alkyloxyC₁-C₆alkyl, C₁-C₆alkylcarbonyl, arylcarbonyl,hetarylcarbonyl, arylC₁-C₆alkylcarbonyl, hetarylC₁-C₆alkylcarbonyl,C₁-C₆alkylcarboxy, arylcarboxy or arylC₁-C₆alkylcarboxy wherein thealkyl and aryl groups independently are optionally substituted with oneor more of R⁷;

R⁷ are independently hydrogen, halo, hydroxy, oxo, nitro, NR⁵R⁶, cyano,COOR⁸, CONR⁵R⁶, C₁-C₈alkyl, C₁-C₆alkyloxy, aryloxy or hetaryloxy;

R⁸ is hydrogen, C₁-C₆alkyl, aryl, arylC₁-C₆alkyl, hetarylalkyl, whereinthe alkyl, aryl and hetarylalkyl groups independently are optionallysubstituted with one or more of R⁷; or

a salt thereof with a pharmaceutically acceptable acid or base, or anyoptical isomer or mixture of optical isomers, including a racemicmixture, or any tautomeric forms.

In one embodiment of the present invention, in formula (VIII) X is NR⁴or S wherein R⁴ is defined as above.

In another embodiment of the present invention, in formula (VIII) X isO.

In another embodiment of the present invention, in formula (VIII) X isS.

In another embodiment of the present invention, in formula (VIII) is NR⁴wherein R⁴ is defined as above.

In another embodiment of the present invention, in formula (VIII) R¹ andR² independently are hydrogen, halo, trihalomethyl or C₁-C₆alkyl,wherein the alkyl groups independently are optionally substituted withone or more of R⁷.

In another embodiment of the present invention, in formula (VIII) R³ ishydrogen, C₁-C₆alkyl, aryl, arylC₁-C₆alkyl, hetaryl or hetarylalkyl,wherein the alkyl, cycloalkyl, aryl, hetaryl and hetarylalkyl groupsindependently are optionally substituted with one or more of R⁷.

In another embodiment of the present invention, in formula (VIII) R⁴ ishydrogen, C₁-C₈alkyl, aryl, hetaryl, hetarylC₁-C₆alkyl, arylC₁-C₆alkyl,wherein the alkyl, aryl, hetaryl, groups independently are optionallysubstituted with one or more of R⁷.

In another embodiment of the present invention, in formula (VIII) R⁵ andR⁶ are together with the nitrogen to which they are attached, forming asaturated or partially saturated cyclic, bicyclic or tricyclic ringsystem containing from 6 to 10 carbon atoms and from 0 to 2 additionalheteroatoms selected from nitrogen, oxygen or sulphur, the ring systemoptionally being substituted with at least one of C₁-C₆alkyl, aryl,hetaryl, arylC₁-C₆alkyl, hetarylalkyl, hydroxy, oxo, cyano,C₁-C₆alkyloxy, arylC₁-C₆alkyloxy, hetarylC₁-C₆alkyloxy,C₁-C₆alkyloxyC₁-C₆alkyl, C₁-C₆alkylcarbonyl, arylcarbonyl,hetarylcarbonyl, arylC₁-C₆alkylcarbonyl, hetarylC₁-C₆alkylcarbonyl,C₁-C₆alkylcarboxy, arylcarboxy or arylC₁-C₆alkylcarboxy wherein thealkyl and aryl groups independently are optionally substituted with oneor more of R⁷.

In yet another embodiment of the present invention, in formula (VIII) R⁵and R⁶, together with the nitrogen to which they are attached, areazepane, azocane, 6-aza-bicyclo[3.2.1]octane,8-aza-bicyclo[3.2.1]octane, 3-aza-bicyclo[3.2.1]octane,2-aza-bicyclo[3.2.1]octane, 3-oxa-6-aza-bicyclo[3.2.1]octane,6-aza-bicyclo[3.2.2]nonane, 3-aza-bicyclo[3.2.2]nonane,4-aza-tricyclo[4.3.1.1^(3,8)]undecane.

In another embodiment of the present invention the compounds of thegeneral formulas (VIII) or a prodrug thereof is selected from the groupconsisting of:

-   (4-Methyl-2-phenyl-thiazol-5-yl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone;-   (2,4-Dimethyl-thiazol-5-yl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone;-   (4-Methyl-2-pyrazin-2-yl-thiazol-5-yl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone;-   [4-Methyl-2-(4-trifluoromethyl-phenyl)-thiazol-5-yl]-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone;-   (3-Aza-bicyclo[3.2.2]non-3-yl)-(2,4-dimethyl-thiazol-5-yl)-methanone;-   (1H-Imidazol-4-yl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone;-   (3-Aza-bicyclo[3.2.2]non-3-yl)-(4-methyl-2-phenyl-thiazol-5-yl)-methanone;-   2,4-Dimethyl-thiazole-5-carboxylic acid cycloheptylamide;-   Azepan-1-yl-(2,4-dimethyl-thiazol-5-yl)-methanone;-   2,4-Dimethyl-thiazole-5-carboxylic acid adamantan-1-ylamide;-   (3-Aza-bicyclo[3.2.2]non-3-yl)-(1H-imidazol-4-yl)-methanone;-   2,4-Dimethyl-thiazole-5-carboxylic acid    (3-hydroxy-adamantan-1-yl)-amide; or    a salt thereof with a pharmaceutically acceptable acid or base, or    any optical isomer or mixture of optical isomers, including a    racemic mixture, or any tautomeric forms.

In another embodiment of the present invention the compounds of thegeneral formulas (VIII) or a prodrug thereof is selected from the groupconsisting of:

-   (1-Methyl-1H-imidazol-4-yl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone;-   [1-(6-Methyl-pyridin-2-yl)-1H-imidazol-4-yl]-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone;-   [1-(4-Chloro-benzyl)-5-methyl-1H-imidazol-4-yl]-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone;    or    a salt thereof with a pharmaceutically acceptable acid or base, or    any optical isomer or mixture of optical isomers, including a    racemic mixture, or any tautomeric forms.

The compounds of the present invention have asymmetric centers and mayoccur as racemates, racemic mixtures, and as individual enantiomers ordiastereoisomers, with all isomeric forms being included in the presentinvention as well as mixtures thereof.

The present invention also encompasses pharmaceutically acceptable saltsof the present compounds. Such salts include pharmaceutically acceptableacid addition salts, pharmaceutically acceptable base addition salts,pharmaceutically acceptable metal salts, ammonium and alkylated ammoniumsalts. Acid addition salts include salts of inorganic acids as well asorganic acids. Representative examples of suitable inorganic acidsinclude hydrochloric, hydrobromic, hydroiodic, phosphoric, sulfuric,nitric acids and the like. Representative examples of suitable organicacids include formic, acetic, trichloroacetic, trifluoroacetic,propionic, benzoic, cinnamic, citric, fumaric, glycolic, lactic, maleic,malic, malonic, mandelic, oxalic, picric, pyruvic, salicylic, succinic,methanesulfonic, ethanesulfonic, tartaric, ascorbic, pamoic,bismethylene salicylic, ethanedisulfonic, gluconic, citraconic,aspartic, stearic, palmitic, EDTA, glycolic, paminobenzoic, glutamic,benzenesulfonic, p-toluenesulfonic acids, sulphates, nitrates,phosphates, perchlorates, borates, acetates, benzoates,hydroxynaphthoates, glycerophosphates, ketoglutarates and the like.Further examples of pharmaceutically acceptable inorganic or organicacid addition salts include the pharmaceutically acceptable salts listedin J. Pharm. Sci., 66, 2 (1977), which is incorporated herein byreference. Examples of metal salts include lithium, sodium, potassium,barium, calcium, magnesium, zinc, calcium salts and the like. Examplesof amines and organic amines include ammonium, methylamine,dimethylamine, trimethylamine, ethylamine, diethylamine, propylamine,butylamine, tetramethylamine, ethanolamine, diethanolamine,triethanolamine, meglumine, ethylenediamine, choline,N,N′-dibenzylethylenediamine, N-benzylphenylethylamine,N-methyl-D-glucamine, guanidine and the like. Examples of cationic aminoacids include lysine, arginine, histidine and the like.

Further, some of the compounds of the present invention may formsolvates with water or common organic solvents. Such solvates areencompassed within the scope of the invention.

The pharmaceutically acceptable salts are prepared by reacting acompound of the present invention with 1 to 4 equivalents of a base suchas sodium hydroxide, sodium methoxide, sodium hydride, potassiumtert-butoxide, calcium hydroxide, magnesium hydroxide and the like, insolvents like ether, THF, methanol, tert-butanol, dioxane, isopropanol,ethanol etc. Mixtures of solvents may be used. Organic bases likelysine, arginine, diethanolamine, choline, guandine and theirderivatives etc. may also be used. Alternatively, acid addition saltswherever applicable are prepared by treatment with acids such ashydrochloric acid, hydrobromic acid, nitric acid, sulfuric acid,phosphoric acid, p-toluenesulphonic acid, methanesulfonic acid, aceticacid, citric acid, maleic acid salicylic acid, hydroxynaphthoic acid,ascorbic acid, palmitic acid, succinic acid, benzoic acid,benzenesulfonic acid, tartaric acid and the like in solvents like ethylacetate, ether, alcohols, acetone, THF, dioxane etc. Mixture of solventsmay also be used.

The stereoisomers of the compounds forming part of this invention may beprepared by using reactants in their single enantiomeric form in theprocess wherever possible or by conducting the reaction in the presenceof reagents or catalysts in their single enantiomer form or by resolvingthe mixture of stereoisomers by conventional methods. Some of thepreferred methods include use of microbial resolution, enzymaticresolution, resolving the diastereomeric salts formed with chiral acidssuch as mandelic acid, camphorsulfonic acid, tartaric acid, lactic acid,and the like wherever applicable or chiral bases such as brucine, (R)-or (S)-phenylethylamine, cinchona alkaloids and their derivatives andthe like. Commonly used methods are compiled by Jaques et al. in“Enantiomers, Racemates and Resolution” (Wiley Interscience, 1981). Morespecifically the compound of the present invention may be converted to a1:1 mixture of diastereomeric amides by treating with chiral amines,aminoacids, aminoalcohols derived from aminoacids; conventional reactionconditions may be employed to convert acid into an amide; thediastereomers may be separated either by fractional crystallization orchromatography and the stereoisomers of compound of formula I may beprepared by hydrolysing the pure diastereomeric amide.

Various polymorphs of the compounds forming part of this invention maybe prepared by crystallization of said compounds under differentconditions. For example, using different solvents commonly used or theirmixtures for recrystallization; crystallizations at differenttemperatures; various modes of cooling, ranging from very fast to veryslow cooling during crystallizations. Polymorphs may also be obtained byheating or melting the compound followed by gradual or fast cooling. Thepresence of polymorphs may be determined by solid probe nmrspectroscopy, ir spectroscopy, differential scanning calorimetry, powderX-ray diffraction or such other techniques.

The invention also encompasses prodrugs of the present compounds, whichon administration undergo chemical conversion by metabolic processesbefore becoming active pharmacological substances. In general, suchprodrugs will be functional derivatives of the present compounds, whichare readily convertible in vivo into the required compound of thepresent invention. Conventional procedures for the selection andpreparation of suitable prodrug derivatives are described, for example,in “Design of Prodrugs”, ed. H. Bundgaard, Elsevier, 1985.

It is a well known problem in drug discovery that compounds, such asenzyme inhibitors, may be very potent and selective in biochemicalassays, yet be inactive in vivo. This lack of so-called bioavailabilitymay be ascribed to a number of different factors such as lack of or poorabsorption in the gut, first pass metabolism in the liver and/or pooruptake in cells. Although the factors determining bioavailability arenot completely understood, there are many examples in the scientificliterature—well known to those skilled in the art—of how to modifycompounds, which are potent and selective in biochemical assays but showlow or no activity in vivo, into drugs that are biologically active.

It is within the scope of the invention to modify the compounds of thepresent invention, termed the ‘original compound’, by attaching chemicalgroups that will improve the bioavailability of said compounds in such away that the uptake in cells or mammals is facilitated.

Examples of said modifications, which are not intended in any way tolimit the scope of the invention, include changing of one or morecarboxy groups to esters (for instance methyl esters, ethyl esters,tert-butyl, acetoxymethyl, pivaloyloxymethyl esters or otheracyloxymethyl esters). Compounds of the invention, original compounds,such modified by attaching chemical groups are termed ‘modifiedcompounds’.

The invention also encompasses active metabolites of the presentcompounds.

The compounds according to the invention alter, and more specifically,reduce the level of active intracellular glucocorticoid and areaccordingly useful for the treatment, prevention and/or prophylaxis ofdisorders and diseases in which such a modulation or reduction isbeneficial.

Accordingly, the present compounds may be applicable for the treatment,prevention and/or prophylaxis of the metabolic syndrome, insulinresistance, dyslipidemia, hypertension, obesity, type 2 diabetes,impaired glucose tolerance (IGT), impaired fasting glucose (IFG), LatentAutoimmune Diabetes in the Adult (LADA), type 1 diabetes, diabetic latecomplications including cardiovascular diseases, cardiovasculardisorders, disorders of lipid metabolism, neurodegenerative andpsychiatric disorders, dysregulation of intraocular pressure includingglaucoma, immune disorders, inappropriate immune responses,musculo-skeletal disorders, gastrointestinal disorders, polycysticovarie syndrome (PCOS), reduced hair growth or other diseases, disordersor conditions that are influenced by intracellular glucocorticoidlevels, adverse effects of increased blood levels of active endogenousor exogenous glucocorticoid, and any combination thereof, adverseeffects of increased plasma levels of endogenous active glucocorticoid,Cushing's disease, Cushing's syndrome, adverse effects of glucocorticoidreceptor agonist treatment of autoimmune diseases, adverse effects ofglucocorticoid receptor agonist treatment of inflammatory diseases,adverse effects of glucocorticoid receptor agonist treatment of diseaseswith an inflammatory component, adverse effects of glucocorticoidreceptor agonist treatment as a part of cancer chemotherapy, adverseeffects of glucocorticoid receptor agonist treatment forsurgical/post-surgical or other trauma, adverse effects ofglucocorticoid receptor agonist therapy in the context of organ ortissue transplantation or adverse effects of glucocorticoid receptoragonist treatment in other diseases, disorders or conditions whereglucocorticoid receptor agonists provide clinically beneficial effects.

More specifically the present compounds may be applicable for thetreatment, prevention and/or prophylaxis of the metabolic syndrome, type2 diabetes, diabetes as a consequence of obesity, insulin resistance,hyperglycemia, prandial hyperglycemia, hyperinsulinemia, inappropriatelylow insulin secretion, impaired glucose tolerance (IGT), impairedfasting glucose (IFG), increased hepatic glucose production, type 1diabetes, LADA, pediatric diabetes, dyslipidemia, diabetic dyslipidemia,hyperlipidemia, hypertriglyceridemia, hyperlipoproteinemia,hypercholesterolemia, decreased HDL cholesterol, impaired LDL/HDL ratio,other disorders of lipid metabolism, obesity, visceral obesity, obesityas a consequence of diabetes, increased food intake, hypertension,diabetic late complications, micro-/macroalbuminuria, nephropathy,retinopathy, neuropathy, diabetic ulcers, cardiovascular diseases,arteriosclerosis, atherosclerosis, coronary artery disease, cardiachypertrophy, myocardial ischemia, heart insufficiency, congestionalheart failure, stroke, myocardial infarction, arrhythmia, decreasedblood flow, erectile dysfunction (male or female), myopathy, loss ofmuscle tissue, muscle wasting, muscle catabolism, osteoporosis,decreased linear growth, neurodegenerative and psychiatric disorders,Alzheimers disease, neuronal death, impaired cognitive function,depression, anxiety, eating disorders, appetite regulation, migraine,epilepsia, addiction to chemical substances, disorders of intraocularpressure, glaucoma, polycystic ovary syndrome (PCOS), inappropriateimmune responses, inappropriate T helper-1/T helper-2 polarisation,bacterial infections, mycobacterial infections, fungal infections, viralinfections, parasitic infestations, suboptimal responses toimmunizations, immune dysfunction, partial or complete baldness, orother diseases, disorders or conditions that are influenced byintracellular glucocorticoid levels and any combination thereof, adverseeffects of glucocorticoid receptor agonist treatment ofallergic-inflammatory diseases such as asthma and atopic dermatitis,adverse effects of glucocorticoid receptor agonist treatment ofdisorders of the respiratory system e.g. asthma, cystic fibrosis,emphysema, bronchitis, hypersensitivity, pneumonitis, eosinophilicpneumonias, pulmonary fibrosis, adverse effects of glucocorticoidreceptor agonist treatment of inflammatory bowel disease such as Crohn'sdisease and ulcerative colitis; adverse effects of glucocorticoidreceptor agonist treatment of disorders of the immune system, connectivetissue and joints e.g. reactive arthritis, rheumatoid arthritis,Sjögren's syndrome, systemic lupus erythematosus, lupus nephritis,Henoch-Schönlein purpura, Wegener's granulomatosis, temporal arteritis,systemic sclerosis, vasculitis, sarcoidosis,dermatomyositis-polymyositis, pemphigus vulgaris; adverse effects ofglucocorticoid receptor agonist treatment of endocrinological diseasessuch as hyperthyroidism, hypoaldosteronism, hypopituitarism; adverseeffects of glucocorticoid receptor agonist treatment of hematologicaldiseases e.g. hemolytic anemia, thrombocytopenia, paroxysmal nocturnalhemoglobinuria; adverse effects of glucocorticoid receptor agonisttreatment of cancer such as spinal cord diseases, neoplastic compressionof the spinal cord, brain tumours, acute lymphoblastic leukemia,Hodgkin's disease, chemotherapy-induced nausea, adverse effects ofglucocorticoid receptor agonist treatment of diseases of muscle and atthe neuro-muscular joint e.g. myasthenia gravis and heriditarymyopathies (e.g. Duchenne muscular dystrophy), adverse effects ofglucocorticoid receptor agonist treatment in the context of surgery &transplantation e.g. trauma, post-surgical stress, surgical stress,renal transplantation, liver transplantation, lung transplantation,pancreatic islet transplantation, blood stem cell transplantation, bonemarrow transplantation, heart transplantation, adrenal glandtransplantation, tracheal transplantation, intestinal transplantation,corneal transplantation, skin grafting, keratoplasty, lens implantationand other procedures where immunosuppression with glucocorticoidreceptor agonists is beneficial; adverse effects of glucocorticoidreceptor agonist treatment of brain absess, nausea/vomiting, infections,hypercalcemia, adrenal hyperplasia, autoimmune hepatitis, spinal corddiseases, saccular aneurysms or adverse effects to glucocorticoidreceptor agonist treatment in other diseases, disorders and conditionswhere glucocorticoid receptor agonists provide clinically beneficialeffects.

Accordingly, in a further aspect the invention relates to a compoundaccording to the invention for use as a pharmaceutical composition.

The invention also relates to pharmaceutical compositions comprising, asan active ingredient, at least one compound according to the inventiontogether with one or more pharmaceutically acceptable carriers ordiluents.

The pharmaceutical composition is preferably in unit dosage form,comprising from about 0.05 mg/day to about 2000 mg/day, preferably fromabout 1 mg/day to about 500 mg/day of a compound according to theinvention.

In another embodiment, the patient is treated with a compound accordingto the invention for at least about 1 week, for at least about 2 weeks,for at least about 4 weeks, for at least about 2 months or for at leastabout 4 months.

In yet another embodiment, the pharmaceutical composition is for oral,nasal, transdermal, pulmonal or parenteral administration.

Furthermore, the invention relates to the use of a compound according tothe invention for the preparation of a pharmaceutical composition forthe treatment, prevention and/or prophylaxis of disorders and diseaseswherein a modulation or an inhibition of the activity of 11βHSD1 isbeneficial.

The invention also relates to a method for the treatment, preventionand/or prophylaxis of disorders and diseases wherein a modulation or aninhibition of the activity of 11βHSD1 is beneficial, the methodcomprising administering to a subject in need thereof an effectiveamount of a compound according to the invention.

In a preferred embodiment of the invention the present compounds areused for the preparation of a medicament for the treatment, preventionand/or prophylaxis of any diseases and conditions that are influenced byintracellular glucocorticoid levels as mentioned above.

Thus, in a preferred embodiment of the invention the present compoundsare used for the preparation of a medicament for the treatment,prevention and/or prophylaxis of conditions and disorders where adecreased level of active intracellular glucocorticoid is desirable,such as the conditions and diseases mentioned above.

In yet a preferred embodiment of the invention the present compounds areused for the preparation of a medicament for the treatment, preventionand/or prophylaxis of the metabolic syndrome including insulinresistance, dyslipidemia, hypertension and obesity.

In yet another preferred embodiment of the invention the presentcompounds are used for the preparation of a medicament for thetreatment, prevention and/or prophylaxis of type 2 diabetes, impairedglucose tolerance (IGT), impaired fasting glucose (IFG).

In yet another preferred embodiment of the invention the presentcompounds are used for the preparation of a pharmaceutical compositionfor the delaying or prevention of the progression from IGT to type 2diabetes.

In yet another preferred embodiment of the invention the presentcompounds are used for the preparation of a pharmaceutical compositionfor the delaying or prevention of the progression of the metabolicsyndrome into type 2 diabetes.

In still another preferred embodiment of the invention the presentcompounds are used for the preparation of a pharmaceutical compositionfor the treatment, prevention and/or prophylaxis of diabetic latecomplications including cardiovascular diseases; arteriosclerosis;atherosclerosis.

In a further preferred embodiment of the invention the present compoundsare used for the preparation of a pharmaceutical composition for thetreatment, prevention and/or prophylaxis of neurodegenerative andpsychiatric disorders.

In yet a further preferred embodiment of the invention the presentcompounds are used for the preparation of a pharmaceutical compositionfor the treatment, prevention and/or prophylaxis of adverse effects ofglucocorticoid receptor agonist treatment or therapy.

In another embodiment of the present invention, the route ofadministration may be any route which effectively transports a compoundaccording to the invention to the appropriate or desired site of action,such as oral, nasal, buccal, transdermal, pulmonal, or parenteral.

In still a further aspect of the invention the present compounds areadministered in combination with one or more further active substancesin any suitable ratios. Such further active substances may e.g. beselected from antiobesity agents, antidiabetics, agents modifying thelipid metabolism, antihypertensive agents, glucocorticoid receptoragonists, agents for the treatment and/or prevention of complicationsresulting from or associated with diabetes and agents for the treatmentand/or prevention of complications and disorders resulting from orassociated with obesity.

Thus, in a further aspect of the invention the present compounds may beadministered in combination with one or more antiobesity agents orappetite regulating agents.

Such agents may be selected from the group consisting of CART (cocaineamphetamine regulated transcript) agonists, NPY (neuropeptide Y)antagonists, MC4 (melanocortin 4) agonists, orexin antagonists, TNF(tumor necrosis factor) agonists, CRF (corticotropin releasing factor)agonists, CRF BP (corticotropin releasing factor binding protein)antagonists, urocortin agonists, β3 agonists, MSH(melanocyte-stimulating hormone) agonists, MCH (melanocyte-concentratinghormone) antagonists, CCK (cholecystokinin) agonists, serotoninre-uptake inhibitors, serotonin and noradrenaline re-uptake inhibitors,mixed serotonin and noradrenergic compounds, 5HT (serotonin) agonists,bombesin agonists, galanin antagonists, growth hormone, growth hormonereleasing compounds, TRH (thyreotropin releasing hormone) agonists, UCP2 or 3 (uncoupling protein 2 or 3) modulators, leptin agonists, DAagonists (bromocriptin, doprexin), lipase/amylase inhibitors, PPAR(peroxisome proliferator-activated receptor) modulators, PXR (retinoid Xreceptor) modulators, TR β agonists, AGRP (Agouti related protein)inhibitors, H3 histamine antagonists, opioid antagonists (such asnaltrexone), exendin-4, GLP-1 and ciliary neurotrophic factor.

In one embodiment of the invention the antiobesity agent is leptin;dexamphetamine or amphetamine; fenfluramine or dexfenfluramine;sibutramine; orlistat; mazindol or phentermine.

Suitable antidiabetic agents include insulin, insulin analogues andderivatives such as those disclosed in EP 792 290 (Novo Nordisk A/S),e.g. N^(εB29)-tetradecanoyl des (B30) human insulin, EP 214 826 and EP705 275 (Novo Nordisk A/S), e.g. Asp^(B28) human insulin, U.S. Pat. No.5,504,188 (Eli Lilly), e.g. Lys^(B28) Pro^(B29) human insulin, EP 368187 (Aventis), eg Lantus, which are all incorporated herein byreference, GLP-1 (glucagon like peptide-1) and GLP-1 derivatives such asthose disclosed in WO 98/08871 to Novo Nordisk A/S, which isincorporated herein by reference as well as orally active hypoglycaemicagents.

The orally active hypoglycaemic agents preferably comprisesulphonylureas, biguanides, meglitinides, glucosidase inhibitors,glucagon antagonists such as those disclosed in WO 99/01423 to NovoNordisk A/S and Agouron Pharmaceuticals, Inc., GLP-1 agonists, potassiumchannel openers such as those disclosed in WO 97/26265 and WO 99/03861to Novo Nordisk A/S which are incorporated herein by reference, DPP-IV(dipeptidyl peptidase-IV) inhibitors, inhibitors of hepatic enzymesinvolved in stimulation of gluconeogenesis and/or glycogenolysis,glucose uptake modulators, compounds modifying the lipid metabolism suchas antihyperlipidemic agents and antilipidemic agents as PPARαmodulators, PPARδ modulators, cholesterol absorption inhibitors, HSL(hormone-sensitive lipase) inhibitors and HMG CoA inhibitors (statins),nicotinic acid, fibrates, anion exchangers, compounds lowering foodintake, bile acid resins, PXR agonists and agents acting on theATP-dependent potassium channel of the β-cells.

In one embodiment, the present compounds are administered in combinationwith insulin or an insulin analogue or derivative, such asN^(εB29)-tetradecanoyl des (B30) human insulin, Asp^(B28) human insulin,Lys^(B28) Pro^(B29) human insulin, Lantus®, or a mix-preparationcomprising one or more of these.

In a further embodiment the present compounds are administered incombination with a sulphonylurea e.g. tolbutamide, glibenclamide,glipizide or glicazide.

In another embodiment the present compounds are administered incombination with a biguanide e.g. metformin.

In yet another embodiment the present compounds are administered incombination with a meglitinide e.g. repaglinide or senaglinide.

In still another embodiment the present compounds are administered incombination with a thiazolidinedione e.g. troglitazone, ciglitazone,pioglitazone, rosiglitazone or compounds disclosed in WO 97/41097 suchas5-[[4-[3-Methyl-4-oxo-3,4-dihydro-2-quinazolinyl]methoxy]phenyl-methyl]thiazolidine-2,4-dioneor a pharmaceutically acceptable salt thereof, preferably the potassiumsalt.

In yet another embodiment the present compounds may be administered incombination with the insulin sensitizers disclosed in WO 99/19313 suchas (−)3-[4-[2-Phenoxazin-10-yl)ethoxy]phenyl]-2-ethoxypropanoic acid ora pharmaceutically acceptable salts thereof, preferably the argininesalt.

In a further embodiment the present compounds are administered incombination with an α-glucosidase inhibitor e.g. miglitol or acarbose.

In another embodiment the present compounds are administered incombination with an agent acting on the ATP-dependent potassium channelof the β-cells e.g. tolbutamide, glibenclamide, glipizide, glicazide orrepaglinide.

Furthermore, the present compounds may be administered in combinationwith nateglinide.

In still another embodiment the present compounds are administered incombination with an antihyperlipidemic agent or antilipidemic agent e.g.cholestyramine, colestipol, clofibrate, gemfibrozil, fenofibrate,bezafibrate, tesaglitazar, EML-4156, LY-818, MK-767, atorvastatin,fluvastatin, lovastatin, pravastatin, simvastatin, acipimox, probucol,ezetimibe or dextrothyroxine.

In a further embodiment the present compounds are administered incombination with more than one of the above-mentioned compounds e.g. incombination with a sulphonylurea and metformin, a sulphonylurea andacarbose, repaglinide and metformin, insulin and a sulphonylurea,insulin and metformin, insulin, insulin and lovastatin, etc.

Further, the present compounds may be administered in combination withone or more antihypertensive agents. Examples of antihypertensive agentsare β-blockers such as alprenolol, atenolol, timolol, pindolol,propranolol, metoprolol, bisoprololfumerate, esmolol, acebutelol,metoprolol, acebutolol, betaxotol, celiprolol, nebivolol, tertatolol,oxprenolol, amusolalul, carvedilol, labetalol, β2-receptor blockers e.g.S-atenolol, OPC-1085, ACE (angiotensin converting enzyme) inhibitorssuch as quinapril, lisinopril, enalapril, captopril, benazepril,perindopril, trandolapril, fosinopril, ramipril, cilazapril, delapril,imidapril, moexipril, spirapril, temocapril, zofenopril, S-5590,fasidotril, Hoechst-Marion Roussel: 100240 (EP 00481522), omapatrilat,gemopatrilat and GW-660511, calcium channel blockers such as nifedipine,felodipine, nicardipine, isradipine, nimodipine, diltiazem, amlodipine,nitrendipine, verapamil, lacidipine, lercanidipine, aranidipine,cilnidipine, clevidipine, azelnidipine, barnidipine, efonodipine,iasidipine, iemildipine, iercanidipine, manidipine, nilvadipine,pranidipine, furnidipine, α-blockers such as doxazosin, urapidil,prazosin, terazosin, bunazosin and OPC-28326, diuretics such asthiazides/sulphonamides (e.g. bendroflumetazide, chlorothalidone,hydrochlorothiazide and clopamide), loop-diuretics (e.g. bumetanide,furosemide and torasemide) and potassium sparing diuretics (e.g.amiloride, spironolactone), endothelin ET-A antagonists such as ABT-546,ambrisetan, atrasentan, SB-234551, CI-1034, S-0139 and YM-598,endothelin antagonists e.g. bosentan and J-104133, renin inhibitors suchas aliskiren, vasopressin V1 antagonists e.g. OPC-21268, vasopressin V2antagonists such as tolvaptan, SR-121463 and OPC-31260, B-typenatriuretic peptide agonists e.g. Nesiritide, angiotensin II antagonistssuch as irbesartan, candesartancilexetil, losartan, valsartan,telmisartan, eprosartan, candesartan, CL-329167, eprosartan, iosartan,olmesartan, pratosartan, TA-606, and YM-358, 5-HT2 agonists e.g.fenoldopam and ketanserin, adenosine A1 antagonists such as naftopidil,N-0861 and FK-352, thromboxane A2 antagonists such as KT2-962,endopeptidase inhibitors e.g. ecadotril, nitric oxide agonists such asLP-805, dopamine D1 antagonists e.g. MYD-37, dopamine D2 agonists suchas nolomirole, n-3 fatty acids e.g. omacor, prostacyclin agonists suchas treprostinil, beraprost, PGE1 agonists e.g. ecraprost, Na+/K+ ATPasemodulators e.g. PST-2238, Potassium channel activators e.g. KR-30450,vaccines such as PMD-3117, Indapamides, CGRP-unigene, guanylate cyclasestimulators, hydralazines, methyldopa, docarpamine, moxonidine,CoAprovel, MondoBiotech-811.

Further reference can be made to Remington: The Science and Practice ofPharmacy, 19^(th) Edition, Gennaro, Ed., Mack Publishing Co., Easton,Pa., 1995.

Furthermore, the present compounds may be administered in combinationwith one or more glucocorticoid receptor agonists. Examples of suchglucocorticoid receptor agonists are betametasone, dexamethasone,hydrocortisone, methylprednisolone, prednisolone, prednisone,beclomethasone, butixicort, clobetasol, flunisolide, flucatisone (andanalogues), momethasone, triamcinolonacetonide, triamcinolonhexacetonideGW-685698, NXC-1015, NXC-1020, NXC-1021, NS-126, P-4112, P-4114,RU-24858 and T-25 series.

It should be understood that any suitable combination of the compoundsaccording to the invention with one or more of the above-mentionedcompounds and optionally one or more further pharmacologically activesubstances are considered to be within the scope of the presentinvention.

Pharmaceutical Compositions

The compounds of the present invention may be administered alone or incombination with pharmaceutically acceptable carriers or excipients, ineither single or multiple doses. The pharmaceutical compositionsaccording to the invention may be formulated with pharmaceuticallyacceptable carriers or diluents as well as any other known adjuvants andexcipients in accordance with conventional techniques such as thosedisclosed in Remington: The Science and Practice of Pharmacy, 19^(th)Edition, Gennaro, Ed., Mack Publishing Co., Easton, Pa., 1995.

The pharmaceutical compositions may be specifically formulated foradministration by any suitable route such as the oral, rectal, nasal,pulmonary, topical (including buccal and sublingual), transdermal,intracisternal, intraperitoneal, vaginal and parenteral (includingsubcutaneous, intramuscular, intrathecal, intravenous and intradermal)route, the oral route being preferred. It will be appreciated that thepreferred route will depend on the general condition and age of thesubject to be treated, the nature of the condition to be treated and theactive ingredient chosen.

Pharmaceutical compositions for oral administration include solid dosageforms such as hard or soft capsules, tablets, troches, dragees, pills,lozenges, powders and granules. Where appropriate, they can be preparedwith coatings such as enteric coatings or they can be formulated so asto provide controlled release of the active ingredient such as sustainedor prolonged release according to methods well-known in the art.

Liquid dosage forms for oral administration include solutions,emulsions, suspensions, syrups and elixirs.

Pharmaceutical compositions for parenteral administration includesterile aqueous and non-aqueous injectable solutions, dispersions,suspensions or emulsions as well as sterile powders to be reconstitutedin sterile injectable solutions or dispersions prior to use. Depotinjectable formulations are also contemplated as being within the scopeof the present invention.

Other suitable administration forms include suppositories, sprays,ointments, crèmes, gels, inhalants, dermal patches, implants etc.

A typical oral dosage is in the range of from about 0.001 to about 100mg/kg body weight per day, preferably from about 0.01 to about 50 mg/kgbody weight per day, and more preferred from about 0.05 to about 10mg/kg body weight per day administered in one or more dosages such as 1to 3 dosages. The exact dosage will depend upon the frequency and modeof administration, the sex, age, weight and general condition of thesubject treated, the nature and severity of the condition treated andany concomitant diseases to be treated and other factors evident tothose skilled in the art.

The formulations may conveniently be presented in unit dosage form bymethods known to those skilled in the art. A typical unit dosage formfor oral administration one or more times per day such as 1 to 3 timesper day may contain from 0.05 to about 2000 mg, e.g. from about 0.1 toabout 1000 mg, from about 0.5 mg to about 500 mg., from about 1 mg toabout 200 mg, e.g. about 100 mg.

For parenteral routes, such as intravenous, intrathecal, intramuscularand similar administration, typically doses are in the order of abouthalf the dose employed for oral administration.

The compounds of this invention are generally utilized as the freesubstance or as a pharmaceutically acceptable salt thereof. Examples arean acid addition salt of a compound having the utility of a free baseand a base addition salt of a compound having the utility of a freeacid. The term “pharmaceutically acceptable salts” refers to non-toxicsalts of the compounds for use according to the present invention whichare generally prepared by reacting the free base with a suitable organicor inorganic acid or by reacting the acid with a suitable organic orinorganic base. When a compound for use according to the presentinvention, contains a free base such salts are prepared in aconventional manner by treating a solution or suspension of the compoundwith a chemical equivalent of a pharmaceutically acceptable acid. When acompounds for use according to the present invention, contains a freeacid such salts are prepared in a conventional manner by treating asolution or suspension of the compound with a chemical equivalent of apharmaceutically acceptable base. Physiologically acceptable salts of acompound with a hydroxy group include the anion of said compound incombination with a suitable cation such as sodium or ammonium ion. Othersalts which are not pharmaceutically acceptable may be useful in thepreparation of compounds for use according to the present invention andthese form a further aspect of the present invention.

For parenteral administration, solutions of the present compounds insterile aqueous solution, aqueous propylene glycol or sesame or peanutoil may be employed. Such aqueous solutions should be suitable bufferedif necessary and the liquid diluent first rendered isotonic withsufficient saline or glucose. The aqueous solutions are particularlysuitable for intravenous, intramuscular, subcutaneous andintraperitoneal administration. The sterile aqueous media employed areall readily available by standard techniques known to those skilled inthe art.

Suitable pharmaceutical carriers include inert solid diluents orfillers, sterile aqueous solution and various organic solvents. Examplesof suitable carriers are water, salt solutions, alcohols, polyethyleneglycols, polyhydroxyethoxylated castor oil, peanut oil, olive oil,syrup, phospholipids, gelatine, lactose, terra alba, sucrose,cyclodextrin, amylose, magnesium stearate, talc, gelatin, agar, pectin,acacia, stearic acid or lower alkyl ethers of cellulose, silicic acid,fatty acids, fatty acid amines, fatty acid monoglycerides anddiglycerides, pentaerythritol fatty acid esters, polyoxyethylene,hydroxymethylcellulose and polyvinylpyrrolidone. Similarly, the carrieror diluent may include any sustained release material known in the art,such as glyceryl monostearate or glyceryl distearate, alone or mixedwith a wax. The formulations may also include wetting agents,emulsifying and suspending agents, preserving agents, sweetening agentsor flavouring agents.

The pharmaceutical compositions formed by combining the compounds of theinvention and the pharmaceutically acceptable carriers are then readilyadministered in a variety of dosage forms suitable for the disclosedroutes of administration. The formulations may conveniently be presentedin unit dosage form by methods known in the art of pharmacy.

Formulations of the present invention suitable for oral administrationmay be presented as discrete units such as capsules or tablets, eachcontaining a predetermined amount of the active ingredient, and whichmay include a suitable excipient. These formulations may be in the formof powder or granules, as a solution or suspension in an aqueous ornon-aqueous liquid, or as an oil-in-water or water-in-oil liquidemulsion.

Compositions intended for oral use may be prepared according to anyknown method, and such compositions may contain one or more agentsselected from the group consisting of sweetening agents, flavouringagents, colouring agents, and preserving agents in order to providepharmaceutically elegant and palatable preparations. Tablets may containthe active ingredient in admixture with non-toxicpharmaceutically-acceptable excipients which are suitable for themanufacture of tablets. These excipients may be for example, inertdiluents, such as calcium carbonate, sodium carbonate, lactose, calciumphosphate or sodium phosphate; granulating and disintegrating agents,for example corn starch or alginic acid; binding agents, for example,starch, gelatine or acacia; and lubricating agents, for examplemagnesium stearate, stearic acid or talc. The tablets may be uncoated orthey may be coated by known techniques to delay disintegration andabsorption in the gastrointestinal tract and thereby provide a sustainedaction over a longer period. For example, a time delay material such asglyceryl monostearate or glyceryl distearate may be employed. They mayalso be coated by the techniques described in U.S. Pat. Nos. 4,356,108;4,166,452; and 4,265,874, incorporated herein by reference, to formosmotic therapeutic tablets for controlled release.

Formulations for oral use may also be presented as hard gelatinecapsules where the active ingredient is mixed with an inert soliddiluent, for example, calcium carbonate, calcium phosphate or kaolin, ora soft gelatine capsule wherein the active ingredient is mixed withwater or an oil medium, for example peanut oil, liquid paraffin, orolive oil.

Aqueous suspensions may contain the active compounds in admixture withexcipients suitable for the manufacture of aqueous suspensions. Suchexcipients are suspending agents, for example sodiumcarboxymethylcellulose, methylcellulose, hydroxypropylmethylcellulose,sodium alginate, polyvinylpyrrolidone, gum tragacanth and gum acacia;dispersing or wetting agents may be a naturally-occurring phosphatidesuch as lecithin, or condensation products of an alkylene oxide withfatty acids, for example polyoxyethylene stearate, or condensationproducts of ethylene oxide with long chain aliphatic alcohols, forexample, heptadecaethyl-eneoxycetanol, or condensation products ofethylene oxide with partial esters derived from fatty acids and ahexitol such as polyoxyethylene sorbitol monooleate, or condensationproducts of ethylene oxide with partial esters derived from fatty acidsand hexitol anhydrides, for example polyethylene sorbitan monooleate.The aqueous suspensions may also contain one or more colouring agents,one or more flavouring agents, and one or more sweetening agents, suchas sucrose or saccharin.

Oily suspensions may be formulated by suspending the active ingredientin a vegetable oil, for example arachis oil, olive oil, sesame oil orcoconut oil, or in a mineral oil such as a liquid paraffin. The oilysuspensions may contain a thickening agent, for example beeswax, hardparaffin or cetyl alcohol. Sweetening agents such as those set forthabove, and flavouring agents may be added to provide a palatable oralpreparation. These compositions may be preserved by the addition of ananti-oxidant such as ascorbic acid.

Dispersible powders and granules suitable for preparation of an aqueoussuspension by the addition of water provide the active compound inadmixture with a dispersing or wetting agent, suspending agent and oneor more preservatives. Suitable dispersing or welting agents andsuspending agents are exemplified by those already mentioned above.Additional excipients, for example, sweetening, flavouring, andcolouring agents may also be present.

The pharmaceutical compositions comprising a compound for use accordingto the present invention may also be in the form of oil-in-wateremulsions. The oily phase may be a vegetable oil, for example, olive oilor arachis oil, or a mineral oil, for example a liquid paraffin, or amixture thereof. Suitable emulsifying agents may be naturally-occurringgums, for example gum acacia or gum tragacanth, naturally-occurringphosphatides, for example soy bean, lecithin, and esters or partialesters derived from fatty acids and hexitol anhydrides, for examplesorbitan monooleate, and condensation products of said partial esterswith ethylene oxide, for example polyoxyethylene sorbitan monooleate.The emulsions may also contain sweetening and flavouring agents.

Syrups and elixirs may be formulated with sweetening agents, for exampleglycerol, propylene glycol, sorbitol or sucrose. Such formulations mayalso contain a demulcent, preservative and flavouring and colouringagent. The pharmaceutical compositions may be in the form of a sterileinjectable aqueous or oleaginous suspension. This suspension may beformulated according to the known methods using suitable dispersing orwetting agents and suspending agents described above. The sterileinjectable preparation may also be a sterile injectable solution orsuspension in a non-toxic parenterally-acceptable diluent or solvent,for example as a solution in 1,3-butanediol. Among the acceptablevehicles and solvents that may be employed are water, Ringer's solution,and isotonic sodium chloride solution. In addition, sterile, fixed oilsare conveniently employed as solvent or suspending medium. For thispurpose, any bland fixed oil may be employed using synthetic mono- ordiglycerides. In addition, fatty acids such as oleic acid find use inthe preparation of injectables.

The compositions may also be in the form of suppositories for rectaladministration of the compounds of the present invention. Thesecompositions can be prepared by mixing the drug with a suitablenon-irritating excipient which is solid at ordinary temperatures butliquid at the rectal temperature and will thus melt in the rectum torelease the drug. Such materials include cocoa butter and polyethyleneglycols, for example.

For topical use, creams, ointments, jellies, solutions of suspensions,etc., containing the compounds of the present invention arecontemplated. For the purpose of this application, topical applicationsshall include mouth washes and gargles.

The compounds for use according to the present invention may also beadministered in the form of liposome delivery systems, such as smallunilamellar vesicles, large unilamellar vesicles, and multilamellarvesicles. Liposomes may be formed from a variety of phospholipids, suchas cholesterol, stearylamine, or phosphatidylcholines.

In addition, some of the compounds for use according to the presentinvention may form solvates with water or common organic solvents. Suchsolvates are also encompassed within the scope of the present invention.

Thus, in a further embodiment, there is provided a pharmaceuticalcomposition comprising a compound for use according to the presentinvention, or a pharmaceutically acceptable salt, solvate, or prodrugthereof, and one or more pharmaceutically acceptable carriers,excipients, or diluents.

If a solid carrier is used for oral administration, the preparation maybe tabletted, placed in a hard gelatine capsule in powder or pellet formor it can be in the form of a troche or lozenge. The amount of solidcarrier will vary widely but will usually be from about 25 mg to about 1g. If a liquid carrier is used, the preparation may be in the form of asyrup, emulsion, soft gelatine capsule or sterile injectable liquid suchas an aqueous or non-aqueous liquid suspension or solution.

A typical tablet which may be prepared by conventional tablettingtechniques may contain: Core: Active compound (as free compound or saltthereof) 5.0 mg Lactosum Ph. Eur. 67.8 mg Cellulose, microcryst.(Avicel) 31.4 mg Amberlite ®IRP88* 1.0 mg Magnesii stearas Ph. Eur. q.s.Coating: Hydroxypropyl methylcellulose approx. 9 mg Mywacett 9-40 T**approx. 0.9 mg*Polacrillin potassium NF, tablet disintegrant, Rohm and Haas.**Acylated monoglyceride used as plasticizer for film coating.

The compounds of the invention may be administered to a patient which isa mammal, especially a human in need thereof. Such mammals include alsoanimals, both domestic animals, e.g. household pets, and non-domesticanimals such as wildlife.

Any novel feature or combination of features described herein isconsidered essential to this invention.

The present invention also relate to the below methods of preparing thecompounds of the invention.

The present invention is further illustrated in the followingrepresentative examples which are, however, not intended to limit thescope of the invention in any way.

EXAMPLES Compounds of General Formulas (I) and (II)

The following examples and general procedures refer to intermediatecompounds and final products for general formula (I) and (II) identifiedin the specification and in the synthesis schemes. The preparation ofthe compounds of general formula (I) and (II) of the present inventionis described in detail using the following examples. Occasionally, thereaction may not be applicable as described to each compound includedwithin the disclosed scope of the invention.

The compounds for which this occurs will be readily recognised by thoseskilled in the art. In these cases the reactions can be successfullyperformed by conventional modifications known to those skilled in theart, which is, by appropriate protection of interfering groups, bychanging to other conventional reagents, or by routine modification ofreaction conditions. Alternatively, other reactions disclosed herein orotherwise conventional will be applicable to the preparation of thecorresponding compounds of the invention. In all preparative methods,all starting materials are known or may easily be prepared from knownstarting materials. The structures of the compounds are confirmed byeither elemental analysis or nuclear magnetic resonance (NMR), wherepeaks assigned to characteristic protons in the title compounds arepresented where appropriate. ¹H NMR shifts (δ_(H)) are given in partsper million (ppm) down field from tetramethylsilane as internalreference standard. M.p.: is melting point and is given in ° C. and isnot corrected. Column chromatography was carried out using the techniquedescribed by W. C. Still et al., J. Org. Chem. 43: 2923 (1978) on Mercksilica gel 60 (Art. 9385). HPLC analyses are performed using 5 μm C184×250 mm column eluted with various mixtures of water and acetonitrile,flow=1 ml/min, as described in the experimental section.

Microwave oven synthesis: The reaction was heated by microwaveirradiation in sealed microwave vessels in a single mode Emrys OptimizerEXP from PersonalChemistry®.

Preparative HPLC: Column: 1.9×15 cm Waters XTerra RP-18. Buffer: lineargradient 5-95% in 15 min, MeCN, 0.1% TFA, flow rate of 15 ml/min. Thepooled fractions are either evaporated to dryness in vacuo, orevaporated in vacuo until the MeCN is removed, and then frozen andfreeze dried.

The abbreviations as used in the examples have the following meaning:

TLC: Thin layer chromatography

CDCl₃: Deuterio chloroform

CD₃OD: Tetradeuterio methanol

DCM: Dichloromethane

DMF: N,N-dimethylformamide

DMSO-d₆: Hexadeuterio dimethylsulfoxide

DMSO: Dimethylsulfoxide

DIPEA: Diisopropylethylamine

EDAC: 1-(3-Dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride

EtOAc: Ethyl acetate

THF: Tetrahydrofuran

DMF: N,N-dimethylformamide

HOBT: 1-Hydroxy-benzotriazole

MeCN: Acetonitrile

NMP: N-Methylpyrrolidinone

TFA: Trifluoroacetic acid

EDAC: 1-(3-Dimethylaminopropyl)-3-ethylcarbodiimide, hydrochloride

min: minutes

hrs: hours

General Method A:

By allowing an acid (I) wherein R³ is defined as above to be coupledwith an amine (II) wherein R¹ and R² are defined as above under standardamide forming conditions using a coupling reagent (III) (e.g. HOBT, EDACand DIPEA in dry THF) affording amide (IV) wherein R¹, R² and R³ aredefined as above.General Method B:

By allowing an acid derivative (I) wherein X is halo, R³(C═O)O—,C₁-C₆alkyloxy or arylC₁-C₆alkyloxy and R³ are defined as above to reactwith an amine (II) wherein R¹ and R² are defined as above under basicconditions (e.g. triethylamine, K₂CO₃, NaH and the like) in a solvent(e.g. THF, DCM, DMF, NMP and the like) affording amide (III); whereinR¹, R² and R³ are defined as above.General Method C:

By allowing an acid derivative (I) wherein X is halo, R²⁰(C═O)O—,C₁-C₆alkyloxy or arylC₁-C₆alkyloxy, R²⁰ is C₁-C₆alkyl or arylC₁-C₆alkyland R³ and X are defined as above to react with an amine (II) wherein R¹and R² are defined as above under basic conditions (e.g. triethylamine,K₂CO₃, NaH and the like) in a solvent (e.g. THF, DCM, DMF, NMP and thelike) affording amide (III); wherein R¹, R² and R³ are defined as above;or when X is hydroxy the acid derivative (I) wherein R³ is as definedabove is coupled with an amine (II) wherein R¹ and R² are defined asabove under standard amide forming conditions using a coupling reagent(a) (e.g. HOBT, EDAC and DIPEA in dry THF) affording amide (III) whereinR¹, R² and R³ are as defined above.

Example 1 General Method (A)4-(Benzo[1,3]-dioxol-5-yloxy)-N-cyclohexyl-N-methyl-butyramide

To a solution of 4-(benzo[1,3]dioxol-5-yloxy)-butyric acid (1.0 g, 4.46mmol), HOBT (0.66 g, 4.91 mmol) in dry THF (75 ml) was added EDAC (0.94g, 4.91 mmol) and the mixture was stirred for 20 minutes. Di-isopropylethyl amine (DIPEA) (860 μl, 4.91 mmol) and cyclohexyl-methyl-amine (555mg, 4.91 mmol) was added and the resulting mixture was stirred for 16hrs. at room temperature. The volatiles were evaporated in vacuo and theresidue was purified by silicagel chromatography using a mixture ofethyl acetate/hexane (1:4) as eluent. Pure fractions were collected andthe solvent evaporated in vacuo to dryness. The oily residuecrystallized on standing affording 1.1 g (77%) of the title compounds asa solid.

¹H NMR (300 MHz, CDCl₃) δ 1.07-1.85 (m, 11H), 2.10 (m, 2H), 2.48 (t,1H), 2.53 (t, 1H), 2.81 and 2.83 (2×s, 3H, N-Me rotamers), 3.96 (t, 2H),5.90 (s, 2H), 6.32 (dd, 1H), 6.49 (d, 1H), 6.69 (d, 1H).

Calculated for C₁₈H₂₅NO₄;

C, 67.69%; H, 7.89%; N, 4.39%. Found:

C, 67.74%; H, 7.99%; N, 4.34%.

Example 2 General Method (A)N-Methyl-N-(1-methyl-piperidin-4-yl)-4-phenoxy-butyramide

To a solution of 4-phenoxy-butyric acid (1.0 g, 5.55 mmol), HOBT (0.83g, 6.1 mmol) in dry THF (75 ml) was added EDAC (1.17 g, 6.1 mmol) andthe mixture was stirred for 20 minutes. Di-isopropyl ethyl amine (DIPEA)(1.06 ml, 6.1 mmol) and methyl-(1-methyl-piperidin-4-yl)amine (783 mg,6.1 mmol) was added and the resulting mixture was stirred for 16 hrs. atroom temperature. The volatiles were evaporated in vacuo and the residuewas purified by silicagel chromatography using a mixture of ethylacetate/triethyl amine (1:25) as eluent. Pure fractions were collectedand the solvent evaporated in vacuo to dryness affording 1.1 g (68%) ofthe title compounds as an oil.

¹H NMR (300 MHz, CDCl₃) δ1.57 (m, 2H), 1.74 (dq, 1H), 1.86-2.18 (m, 5H),2.28 (t, 3H), 2.52 (m, 2H), 2.82 and 2.85 (2×s, 3H, N-Me rotamers), 2.89(bd, 2H), 3.60 and 4.51 (2×dt, 1H), 4.04 (t, 2H), 6.91 (m, 3H), 7.28 (m,2H).

Calculated for C₁₇H₂₆N₂O₂;

C, 70.31%; H, 9.02%; N, 9.65%. Found:

C, 69.72%; H, 9.29%; N, 10.12%.

Example 3 General Method (A) Azepan-1-yl-(3-chloro-phenyl)-methanone

To a solution of 3-chloro benzoic acid (1.0 g, 6.39 mmol), HOBT (0.95 g,7.03 mmol) in dry THF (50 ml) was added EDAC (1.35 g, 7.03 mmol) and themixture was stirred for 20 minutes. Di-isopropyl ethyl amine (DIPEA)(1.22 ml, 7.03 mmol) and azepane (697 mg, 7.03 mmol) was added and theresulting mixture was stirred for 4 hrs. at room temperature. Thevolatiles were evaporated in vacuo, water (50 ml) was added, theresulting mixture extracted with diethyl ether (2×25 ml), dried(Na₂SO₄), filtered and evaporated in vacuo. The residue was purified bysilicagel chromatography using a mixture of ethyl acetate/heptane (1:1)as eluent. Pure fractions were collected and the solvent evaporated invacuo to dryness affording 0.9 g (59%) of the title compounds as an oil.

¹H NMR (300 MHz, CDCl₃) δ 1.61 (m, 6H), 1.84 (m, 2H), 3.35 (t, 2H), 3.67(t, 2H), 7.23-7.39 (m, 4H).

Example 4 General Procedure C(4-Tetrazol-1-yl-phenyl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone

To a mixture of 4-(1H-tetrazol-5-yl)-benzoic acid (0.5 g, 2.63 mmol) andHOBT (0.39 g, 2.89 mmol) in dry THF (35 mL) was added EDAC (0.55 g, 2.89mmol). The resulting mixture was stirred for 10 min. followed byaddition of a mixture of DIPEA (0.50 ml, 2.89 mmol) and1,3,3-trimethyl-6-aza-bicyclo[3.2.1]octane (0.49 ml, 2.89 mmol). Thereaction mixture was stirred for an additional 6 hrs. and evaporated todryness. To the residue was added water (10 ml) and the resultingmixture was extracted with diethyl ether (2×10 ml). The combined organicphases were dried (Na₂SO₄), filtered and evaporated in vacuo. Theresulting residue was purified by column chromatography (silica gel)using a mixture of EtOAc-Heptane (1:2) as eluent. Pure fractions werecollected and evaporated to dryness. To the residue was added diethylether (5 ml) and the precipitate was filtered off, washed with diethylether and dried in vacuo at 50° C. affording 220 mg (26%) of the titlecompound as a solid.

TLC: EtOAc-Heptan (2:1), R_(f): 0.18

¹H-NMR (300 MHz, CDCl₃) δ 0.95-1.15 (m, 9H), 1.21-1.64 (m, 5.5H), 2.25(m, 0.5H), 3.17-3.32 (m, 1.5H), 3.63 (d, 0.5H), 3.98 and 4.60 (2×t, 1H),7.68 (t, 2H), 7.78 (m, 2H), 9.06 (s, 1H).

The following compounds were made in a similar way as described inexample 4 above: No Molecule MW IUPAC Name 4-1

323.43 N-Cyclohexyl-N-methyl-2-phenoxymethyl- benzamide 4-2

232.32 4-Amino-N-cyclohexyl-N-methyl-benzamide 4-3

337.46 N-Cycloheptyl-N-methyl-2-phenoxymethyl- benzamide 4-4

217.31 N-Cyclohexyl-N-methyl-benzamide 4-5

269.74 2-Chloro-N-cyclohexyl-6-fluoro-N-methyl- benzamide 4-6

301.31 N-Cyclohexyl-N-methyl-4-trifluoromethoxy- benzamide 4-7

245.36 N-Cyclohexyl-2,3,N-trimethyl-benzamide 4-8

286.20 3,5-Dichloro-N-cyclohexyl-N-methyl-benzamide 4-9

309.41 N-Cyclohexyl-N-methyl-2-phenoxy-benzamide 4-10

429.56 2,4-Bis-benzyloxy-N-cyclohexyl-N-methyl- benzamide 4-11

323.43 2-Benzyloxy-N-cyclohexyl-N-methyl-benzamide 4-12

309.41 N-Cyclohexyl-N-methyl-4-phenoxy-benzamide 4-13

323.43 4-Benzyloxy-N-cyclohexyl-N-methyl-benzamide 4-14

323.43 N-Cyclohexyl-N-methyl-4-phenoxymethyl- benzamide 4-15

310.78 2-Chloro-N-cyclohexyl-N-ethyl-4-nitro- benzamide 4-16

310.78 4-Chloro-N-cyclohexyl-N-ethyl-3-nitro- benzamide 4-17

293.34 6-Fluoro-4H-benzo[1,3]dioxine-8-carboxylic acidcyclohexyl-methyl-amide 4-18

237.73 Azepan-1-yl-(2-chloro-phenyl)-methanone 4-19

237.73 Azepan-1-yl-(3-chloro-phenyl)-methanone 4-20

203.28 Azepan-1-yl-phenyl-methanone 4-21

385.51 2-(Biphenyl-4-yloxy)-N-cyclohexyl-N-methyl- benzamide 4-22

369.46 N-Cyclohexyl-2-(3,5-dimethoxy-phenoxy)-N- methyl-benzamide 4-23

369.46 N-Cyclohexyl-2-(2,3-dimethoxy-phenoxy)-N- methyl-benzamide 4-24

386.32 2,4-Dichloro-N-(3,3-dimethyl-1,5-dioxa-spiro[5.5]undec-9-yl)-N-methyl-benzamide 4-25

300.18 2,4-Dichloro-N-methyl-N-(4-oxo-cyclohexyl)- benzamide 4-26

233.31 N-Cyclohexyl-2-hydroxy-N-methyl-benzamide 4-27

247.34 N-Cyclohexyl-3-methoxy-N-methyl-benzamide 4-28

261.32 Benzo[1,3]dioxole-5-carboxylic acid cyclohexyl- methyl-amide 4-29

323.43 3-Benzyloxy-N-cyclohexyl-N-methyl-benzamide 4-30

233.31 N-Cyclohexyl-3-hydroxy-N-methyl-benzamide 4-31

406.54 [4-(Morpholine-4-sulfonyl)-phenyl]-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)- methanone 4-32

426.58 N-Benzyl-3-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]octane-6-carbonyl)- benzenesulfonamide 4-33

424.53 [4-Fluoro-3-(morpholine-4-sulfonyl)-phenyl]-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)- methanone 4-34

418.58 Thiophene-2-sulfonic acid [4-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]octane-6-carbonyl)-phenyl]- amide 4-35

412.55 N-Phenyl-4-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]octane-6-carbonyl)- benzenesulfonamide 4-36

349.47 (4-Phenoxy-phenyl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone 4-37

440.60 N-(2,4-Dimethyl-phenyl)-3-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]octane-6-carbonyl)- benzenesulfonamide 4-38

363.50 (2-Phenoxymethyl-phenyl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone 4-39

392.56 4-(3-Aza-bicyclo[3.2.2]nonane-3-carbonyl)-N,N-dipropyl-benzenesulfonamide 4-40

296.21 2-Bromo-N-cyclohexyl-N-methyl-benzamide 4-41

314.43 N-[4-(1,3,3-Trimethyl-6-aza-bicyclo[3.2.1]octane-6-carbonyl)-phenyl]- acetamide 4-42

300.44 (4-Dimethylamino-phenyl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone 4-43

322.45 (4-Pyrrol-1-yl-phenyl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone 4-44

323.44 (4-Imidazol-1-yl-phenyl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone 4-45

302.42 (4-Amino-2-methoxy-phenyl)-(trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone 4-46

335.46 (4-Methanesulfonyl-phenyl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone 4-47

335.46 (3-Methanesulfonyl-phenyl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone 4-48

397.54 (4-Benzenesulfonyl-phenyl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone 4-49

348.49 Azepan-1-yl-[4-(3,4-dihydro-1H-isoquinolin-2-ylmethyl)-phenyl]-methanone 4-50

302.42 Azepan-1-yl-(4-morpholin-4-ylmethyl-phenyl)- methanone 4-51

391.44 [4-(3-Trifluoromethyl-pyrazol-1-yl)-phenyl]-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)- methanone 4-52

324.42 (4-[1,2,4]Triazol-1-yl-phenyl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone 4-53

323.44 (4-Pyrazol-1-yl-phenyl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone 4-54

337.46 2-Benzyloxymethyl-N-cyclohexyl-N-methyl- benzamide 4-55

313.40 N-Cyclohexyl-N-methyl-4-(3-methyl-5-oxo-4,5-dihydro-pyrazol-1-yl)-benzamide 4-56

353.46 5-Methyl-2-[4-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]octane-6-carbonyl)-phenyl]-2,4- dihydro-pyrazol-3-one 4-57

346.47 (9H-Carbazol-3-yl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone 4-58

351.49 [4-(3,5-Dimethyl-pyrazol-1-yl)-phenyl]-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)- methanone 4-59

257.37 Phenyl-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct- 6-yl)-methanone4-60

282.18 Azepan-1-yl-(2-bromo-phenyl)-methanone 4-61

308.22 (3-Aza-bicyclo[3.2.2]non-3-yl)-(2-bromo-phenyl)- methanone 4-62

330.43 (4-Benzyl-piperidin-1-yl)-quinolin-2-yl- methanone 4-63

254.33 (2-Methyl-piperidin-1-yl)-quinolin-2-yl- methanone 4-64

280.37 (3-Aza-bicyclo[3.2.2]non-3-yl)-quinolin-2-yl- methanone 4-65

268.36 Quinoline-2-carboxylic acid cyclohexyl-methyl- amide 4-66

308.42 Quinolin-2-yl-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone 4-67

354.45 1-[4-(1,3,3-Trimethyl-6-aza-bicyclo[3.2.1]octane-6-carbonyl)-phenyl]-pyrrolidine-2,5-dione 4-68

258.36 Pyridin-3-yl-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone 4-69

258.36 Pyridin-4-yl-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone 4-70

258.36 Pyridin-2-yl-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone 4-71

324.42 (6-Pyrazol-1-yl-pyridin-3-yl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone 4-72

301.38 4-(1,3,3-Trimethyl-6-aza-bicyclo[3.2.1]octane-6-carbonyl)-benzoic acid 4-73

303.4 Imidazo[2,1-b]thiazol-6-yl-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone

Example 5 General Procedure C8-(4-Dimethylamino-benzoyl)-8-aza-bicyclo[3.2.1]octan-3-one

To a mixture of 8-aza-bicyclo[3.2.1]octane (1.8 g, 14.38 mmol), dry THF(75 ml) and TEA (4 ml, 28.76 mmol) was added dropwise a solution of4-dimethylamino-benzoyl chloride (3.17 g, 17.26 mmol) in dry THF (75ml). The resulting mixture was stirred for 1 hr. at room temperaturefollowed by filtration and evaporation in vacuo. The residue waspurified by column chromatography (silica gel) using a mixture ofEtOAc-Heptane (1:2) as eluent. Pure fractions were collected andevaporated to dryness. The residue was crystallized from diethyl ether(25 ml), filtered off and dried in vacuo at 50° C. affording 1.9 g (48%)of the title compound as a solid.

TLC: EtOAc-Heptane (3:1), R_(f): 0.4

¹H-NMR (300 MHz, CDCl₃) δ 1.74 (m, 2H), 2.15 (m, 2H), 2.39 (d, 2H), 2.27(bs, 2H), 3.02 (s, 6H), 4.80 (bs, 2H), 6.68 (d, 2H), 7.50 (d, 2H).

Example 6 General Procedure C(4-Dimethylamino-phenyl)-(3-hydroxy-8-aza-bicyclo[3.2.1]oct-8-yl)-methanone

To a solution of8-(4-dimethylamino-benzoyl)-8-aza-bicyclo[3.2.1]octan-3-one (2.0 g, 7.34mmol) in MeOH (75 ml) was added NaBH₄ (0.45 g, 11.02 mmol, pellets). Theresulting mixture was stirred for 18 hrs, evaporated and to the residuewas added water (75 ml). The aqueous phase was acidified to pH 1 withconc. HCl and washed with diethyl ether (50 ml). The aqueous phase wasneutralized to pH 7 with 1N NaOH. The precipitate was filtered off andwashed with water, diethyl ether and dried in vacuo at 50° C. affording1.15 g (57%) of the title compound as a solid.

¹H-NMR (400 MHz, CDCl₃) δ 1.66-1.95 (m, 6H), 2.22 (d, 2H), 2.99 (s, 6H),4.17 (m, 1H), 4.22 (bs, 1H), 4.74 (bs, 1H), 6.66 (d, 2H), 7.41 (d, 2H).

Example 7 General Procedure C(4-Dimethylamino-phenyl)-(3-hydroxy-3-methyl-8-aza-bicyclo[3.2.1]oct-8-yl)-methanone

To a solution of8-(4-dimethylamino-benzoyl)-8-aza-bicyclo[3.2.1]octan-3-one (200 mg,0.734 mmol) in dry THF (40 ml) was added dropwise a solution ofmethylmagnesium bromide (0.74 ml, 2.20 mmol, 3M in diethyl ether). Theresulting mixture was stirred for 36 hrs. at room temperature andquenched by addition of saturated aqueous ammonium chloride (50 ml). Theaqueous phase was extracted with EtOAc (2×100 ml) and the combinedorganic phases were dried (Na₂SO₄), filtered and evaporated in vacuo.The residue was purified by column chromatography (silica gel) using amixture of EtOAc-Heptane (5:1) as eluent. Pure fractions were collectedand evaporated to dryness affording 45 mg (21%) of the title compound asa solid. TLC: EtOAc, R_(f): 0.39

¹H-NMR (400 MHz, CDCl₃) δ 1.21 (s, 3H), 1.75 (d, 2H), 1.92 (m, 2H), 2.15(bs, 1H), 2.22 (d, 2H), 3.0 (s, 6H), 4.26 (bs, 1H), 4.77 (bs, 1H), 6.66(d, 2H), 7.42 (d, 2H).

Example 8 General Procedure C Trifluoro-acetic acid8-(4-dimethylamino-benzoyl)-8-aza-bicyclo[3.2.1]oct-3-yl ester

NaBH₄ (0.3 g, 2 pellets) was added to TFA (20 ml) at 0° C. and stirredfor 30 min. To this mixture was added a solution of8-(4-dimethylamino-benzoyl)-8-aza-bicyclo[3.2.1]octan-3-one (0.3 g,1.102 mmol) in DCM (10 ml). The resulting mixture was stirred for 64hrs. at room temperature, the volatiles evaporated and to the residuewas added water (10 ml). The aqueous phase was neutralized to pH 7 with1N NaOH and extracted with diethyl ether (2×25 ml). The combined organicphases were evaporated in vacuo and the residue purified by columnchromatography (silica gel) using a mixture of EtOAc-Heptane (1:2) aseluent. Pure fractions were collected and evaporated to drynessaffording 25 mg (9%) of the title compound as a solid. TLC:EtOAc-Heptane (2:1), R_(f): 0.54

LC/MS: m/z: 371H⁺

¹H-NMR (400 MHz, CDCl₃) δ 1.81-1.94 (m, 2H), 2.05 (s, 4H), 2.31 (bs,2H), 3.01 (s, 6H), 4.59 (bs, 2H), 5.35 (t, 1H), 6.67 (d, 2H), 7.42 (d,2H).

EXAMPLES Compounds of General Formula (III)

The following examples and general procedures refer to intermediatecompounds and final products for general formula (III) identified in thespecification and in the synthesis schemes. The preparation of thecompounds of general formula (III) of the present invention is describedin detail using the following examples. Occasionally, the reaction maynot be applicable as described to each compound included within thedisclosed scope of the invention. The compounds for which this occurswill be readily recognised by those skilled in the art. In these casesthe reactions can be successfully performed by conventionalmodifications known to those skilled in the art, that is, by appropriateprotection of interfering groups, by changing to other conventionalreagents, or by routine modification of reaction conditions.Alternatively, other reactions disclosed herein or otherwiseconventional will be applicable to the preparation of the correspondingcompounds of the invention. In all preparative methods, all startingmaterials are known or may easily be prepared from known startingmaterials. The structures of the compounds are confirmed by eitherelemental analysis or nuclear magnetic resonance (NMR), where peaksassigned to characteristic protons in the title compounds are presentedwhere appropriate. ¹H NMR shifts (8H) are given in parts per million(ppm) down field from tetramethylsilane as internal reference standard.M.p.: is melting point and is given in ° C. and is not corrected. Columnchromatography was carried out using the technique described by W. C.Still et al., J. Org. Chem. 43: 2923 (1978) on Merck silica gel 60 (Art.9385). HPLC analyses are performed using 5 μm C18 4×250 mm column elutedwith various mixtures of water and acetonitrile, flow=1 ml/min, asdescribed in the experimental section.

The abbreviations as used in the examples have the following meaning:

TLC: thin layer chromatography

CDCl₃: deuterio chloroform

CD₃OD: tetradeuterio methanol

DMSO-d₆: hexadeuterio dimethylsulfoxide

DMSO: dimethylsulfoxide

THF: tetrahydrofuran

DMF: N,N-dimethylformamide

HOBT: 1-hydroxy-benzotriazole

EDAC: 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide, hydrochloride

min: minutes

hrs: hours

The compounds of the invention are prepared as illustrated in thefollowing reaction scheme 1:

General Method:

By allowing 2,2-dimethyl-1,3-dioxane-4,6-dione (Meldrum's acid) (I) toreact with an acid chloride (II), wherein R² is defined above, in asolvent mixture of pyridine and DCM and the like affording an acylMeldrum's acid (III), wherein R² is as defined above. The acyl Meldrum'sacid (III) is aminolysed with an substituted amine (IV), wherein R³ andR⁴ are defined above, in a solvent such as benzene, toluene, dioxane,and the like at a temperature interval from 50° C. up to refluxaffording a beta-keto amide (V) wherein R², R³ and R⁴ are as definedabove. The beta-keto amide (V) is treated with ortho-formiate (VI) in asolvent such as acetic acid anhydride and the like at a temperatureinterval from 50° C. up to reflux affording enol ether (VII) wherein R²,R³, and R⁴ are as defined above. Condensation of the enol ether (VII)wherein R², R³, and R⁴ are as defined above with hydrazide (VIII)wherein R¹ is as defined above yields pyrazole (IX) wherein R¹, R², R³,and R⁴ are as defined above, in a solvent such as EtOH, i-PrOH,tert-BuOH and the like.

Example 1 1-(4-Chloro-phenyl)-5-propyl-1H-pyrazole-4-carboxylic acidcyclohexyl-methyl-amide

To a solution of 1-(4-chloro-phenyl)-5-propyl-1H-pyrazole-4-carboxylicacid (1.0 g, 3.78 mmol), HOBT (0.56 g, 4.16 mmol) in dry THF (50 ml) wasadded EDAC (0.8 g, 4.16 mmol) and the mixture was stirred for 10minutes. Di-isopropyl ethyl amine (DIPEA) (724 μl, 4.16 mmol) andcyclohexyl-methyl-amine (0.54 ml, 4.16 mmol) was added and the resultingmixture was stirred for 16 hrs. at room temperature. The volatiles wereevaporated in vacuo and the residue was purified by silicagelchromatography using a mixture of ethyl acetate and heptane (1:4) aseluent. Pure fractions were collected and the solvent evaporated invacuo affording 1.1 g (81%) of the title compounds as an oil.

¹H NMR (300 MHz, CDCl₃) δ 0.81 (t, 3H), 1.1-1.86 (m, 13H), 2.81 (t, 2H),2.98 (s, 3H), 3.89 and 4.50 (2×bs, 1H), 7.37 (m, 2H), 7.47 (m, 2H), 7.58(bs, 1H).

Calculated for C₂₀H₂₆ClN₃O, 0.4H₂O; C, 65.44%; H, 7.36%; N, 11.45%.Found: C, 65.47%; H, 7.89%; N, 11.56%.

The following compound was made in a similar way as described in example1 above

Example 2 1-(4-Chloro-phenyl)-5-trifluoromethyl-1H-pyrazole-4-carboxylicacid cyclohexyl-methyl-amide

Calculated for C₁₈H₁₉ClF₃N₃O;

C, 56.04%; H, 4.96%; N, 10.89%. Found:

C, 56.02%; H, 5.16%; N, 10.76%.

Example 3[1-(4-Methoxy-phenyl)-5-methyl-1H-pyrazol-4-yl]-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone

¹H NMR (400 MHz, CDCl₃) δ 0.97 (t, 5H), 1.11 (t, 4H), 1.25-1.61 (m, 4H),1.79 (m, 2H), 2.20 (d, 0.5H), 2.44 (d, 3H), 3.29 (d, 0.5H), 3.40 (d,0.5H), 3.59 (m, 0.5H), 3.86 (s, 3H), 4.37 (m, 0.5H), 4.60 (m, 0.5H),6.99 (d, 2H), 7.33 (d, 2H), 7.74 (s, 1H).

EXAMPLES Compounds of General Formula (IV)

The following examples and general procedures refer to intermediatecompounds and final products for general formula (IV) identified in thespecification and in the synthesis schemes. The preparation of thecompounds of general formula (IV) of the present invention is describedin detail using the following examples. Occasionally, the reaction maynot be applicable as described to each compound included within thedisclosed scope of the invention. The compounds for which this occurswill be readily recognised by those skilled in the art. In these casesthe reactions can be successfully performed by conventionalmodifications known to those skilled in the art, that is, by appropriateprotection of interfering groups, by changing to other conventionalreagents, or by routine modification of reaction conditions.Alternatively, other reactions disclosed herein or otherwiseconventional will be applicable to the preparation of the correspondingcompounds of the invention. In all preparative methods, all startingmaterials are known or may easily be prepared from known startingmaterials. The structures of the compounds are confirmed by eitherelemental analysis or nuclear magnetic resonance (NMR), where peaksassigned to characteristic protons in the title compounds are presentedwhere appropriate. ¹H NMR shifts (6H) are given in parts per million(ppm) down field from tetramethylsilane as internal reference standard.M.p.: is melting point and is given in ° C. and is not corrected. Columnchromatography was carried out using the technique described by W. C.Still et al., J. Org. Chem. 43: 2923 (1978) on Merck silica gel 60 (Art.9385). HPLC analyses are performed using 5 μm C18 4×250 mm column elutedwith various mixtures of water and acetonitrile, flow=1 ml/min, asdescribed in the experimental section.

The abbreviations as used in the examples have the following meaning:

TLC: Thin layer chromatography

CDCl₃: Deuterio chloroform

CD₃OD: Tetradeuterio methanol

DMSO-d₆: Hexadeuterio dimethylsulfoxide

DMSO: Dimethylsulfoxide

THF: Tetrahydrofuran

DMF: N,N-Dimethylformamide

HOBT: 1-Hydroxy-benzotriazole

EDAC: 1-(3-Dimethylaminopropyl)-3-ethylcarbodiimide, hydrochloride

min: minutes

hrs: hours

The compounds of the invention are prepared as illustrated in thefollowing reaction scheme 1:

General Method:

By allowing a N-aminopyridinium iodide (I), wherein R², R³, R⁴ and R⁵are as defined, above to react with a propiolate (II), wherein alkyl andR¹ are as defined above, in a solvent such as DMF and the like, with asuitable base, such as potassium carbonate and the like affording apyrazolo[1,5-a]pyridine-3-carboxylic acid ester (III), wherein R¹, R²,R³, R⁴, R⁵ and alkyl are as defined above. Thepyrazolo[1,5-a]pyridine-3-carboxylic acid ester (III) is hydrolysed witha base affording a pyrazolo[1,5-a]pyridine-3-carboxylic acid (IV),wherein R¹, R², R³, R⁴ and R⁵ are as defined above. Thepyrazolo[1,5-a]pyridine-3-carboxylic acid (IV) is coupled with an amine(V), wherein R⁶ and R⁷ are as defined above, under standard amideforming conditions (e.g. HOBT, EDAC and DIPEA in dry THF) affordingpyrazolo[1,5-a]pyridine-3-amide (VI), wherein R¹, R², R³, R⁴, R⁵, R⁶ andR⁷ are as defined above.

Example 1Pyrazolo[1,5-a]pyridin-3-yl-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone

A solution of pyrazolo[1,5-A]pyridine-3-carboxylic acid (97 mg, 0.6mmol), HOBT (89 mg, 0.66 mmol), EDAC (126 mg, 0.66 mmol) anddi-isopropyl ethyl amine (DIPEA) (115 μl, 0.66 mmol) in dry THF (10 ml)was stirred for 1 hr. and 1,3,3-trimethyl-6-aza-bicyclo[3.2.1]octane(101 mg, 0.66 mmol) was added. The mixture was stirred for 16 hrs. atroom temperature. The mixture was quenched by addition of water (30 ml),extracted with EtOAc (2×50 ml), dried (MgSO₄), filtered and evaporatedin vacuo. The crude product was stirred with water (10 ml) for 30 min.,filtered off and dried in vacuo affording 130 mg (73%) of the titlecompound as a white solid.

¹H NMR (400 MHz, CDCl₃) δ 0.95 (s, 3H), 1.05 (d, 3H), 1.15 (d, 3H),1.36-1.88 (m, 5.5H), 2.23 (d, 0.5H), 3.37 (d, 0.5H), 3.51 (d, 0.5H),3.61 (d, 0.5H), 3.73 (d, 0.5H), 4.56 (m, 0.5H), 4.71 (m, 0.5H), 6.92 (m,1H), 7.33 (m, 1H), 8.19 (s, 1H), 8.47 (m, 2H

The following compounds were made in a similar way was described inexample 1 above.

Example 2(2-Methyl-pyrazolo[1,5-a]pyridin-3-yl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone

¹H NMR (400 MHz, CDCl₃) δ 0.88 (s, 3H), 1.00 (d, 3H), 1.14 (d, 3H),1.22-1.45 (m, 3.5H), 1.58 (d, 0.5H), 1.80-1.90 (m, 1.5H), 2.40 (d,0.5H), 2.50 (s, 3H), 3.20 (dd, 1.5H), 3.82 (d, 0.5H), 4.02 (m, 0.5H),4.57 (m, 0.5H), 6.75 (t, 1H), 7.18 (t, 1H), 7.38 (t, 1H), 8.36 (d, 1H).

Example 3 Pyrazolo[1,5-a]pyridine-3-carboxylic acidcyclohexyl-methyl-amide

¹H NMR (400 MHz, CDCl₃) δ 1.12 (m, 1H), 1.39 (m, 2H), 1.57-1.70 (m, 3H),1.83 (m, 4H), 3.07 (bs, 3H), 4.30 (bs, 1H), 6.89 (t, 1H), 7.30 (d, 1H),8.08 (m, 2H), 8.48 (d, 1H).

EXAMPLES Compounds of General Formula (V)

The following examples and general procedures refer to intermediatecompounds and final products for general formulas (V) and (Va)identified in the specification and in the synthesis schemes. Thepreparation of the compounds of general formulas (V) and (Va) of thepresent invention is described in detail using the following examples.Occasionally, the reaction may not be applicable as described to eachcompound included within the disclosed scope of the invention. Thecompounds for which this occurs will be readily recognised by thoseskilled in the art. In these cases the reactions can be successfullyperformed by conventional modifications known to those skilled in theart, that is, by appropriate protection of interfering groups, bychanging to other conventional reagents, or by routine modification ofreaction conditions. Alternatively, other reactions disclosed herein orotherwise conventional will be applicable to the preparation of thecorresponding compounds of the invention. In all preparative methods,all starting materials are known or may easily be prepared from knownstarting materials. The structures of the compounds are confirmed byeither elemental analysis or nuclear magnetic resonance (NMR), wherepeaks assigned to characteristic protons in the title compounds arepresented where appropriate. ¹H NMR shifts (δ_(H)) are given in partsper million (ppm) down field from tetramethylsilane as internalreference standard. M.p.: is melting point and is given in ° C. and isnot corrected. Column chromatography was carried out using the techniquedescribed by W. C. Still et al., J. Org. Chem. 43: 2923 (1978) on Mercksilica gel 60 (Art. 9385). HPLC analyses are performed using 5 μm C184×250 mm column eluted with various mixtures of water and acetonitrile,flow=1 ml/min, as described in the experimental section.

The abbreviations as used in the examples have the following meaning:

TLC: Thin layer chromatography

CDCl₃: Deuterio chloroform

CD₃OD: Tetradeuterio methanol

DIPEA: Diisopropylethyl amine

DMSO-d₆: Hexadeuterio dimethylsulfoxide

DMSO: Dimethylsulfoxide

THF: Tetrahydrofuran

DMF: N,N-dimethylformamide

HOBT: 1-Hydroxy-benzotriazole

EDAC: 1-(3-Dimethylaminopropyl)-3-ethylcarbodiimide, hydrochloride

min: minutes

hrs: hours

The compounds of the invention are prepared as illustrated in thefollowing reaction schemes:

General Method A

Benzimidazol carboxylic acids (I) wherein R¹, R², R³, R⁵, R⁶ and R⁷ areas defined above are generally prepared as described in the followingliterature references;

-   Sekikawa; Bull. Chem. Soc. Jpn. 31, (1958), 252.-   Zehra; Chem. Ber. 23, (1890), 3629.-   Palmer, B. D. et al.; J. Med. Chem. 41, (1998), 5457-5465.-   Chi, Y.-C. and Sun, C.-M.; Syn. Lett. 5, (2000), 591-594.-   Wu, Z. et al.; Tetrahedron Lett. 41, (2000), 9871-9874.

By allowing an acid (I) wherein R¹, R², R³, R⁵, R⁶ and R⁷ are as definedabove to be coupled with an amine (II) wherein R¹ and R² are defined asabove under standard amide forming conditions using a coupling reagent(a) (e.g. HOBT, EDAC and DIPEA in dry THF) affording amide (III) whereinR¹, R², R³, R⁴, R⁵, X, Y and Z are as defined above.General Method B

By allowing an acid derivative (I) wherein X is halo, R⁸(C═O)O—,C₁-C₆alkyloxy or arylC₁-C₆alkyloxy, R⁸ is C₁-C₆alkyl or arylC₁-C₆alkyland R¹, R², R³, R⁵, R⁶ and R⁷ are defined as above to react with anamine (II) wherein R⁶ and R⁷ are defined as above under basic conditions(e.g. triethylamine, K₂CO₃, NaH and the like) in a solvent (e.g. THF,DCM, DMF, NMP and the like) affording amide (III); wherein R¹, R², R³,R⁴, R⁵, R⁶ and R⁷ are defined as above.

General Method A

Benzimidazol carboxylic acids (I) wherein R¹, R², R³, R⁵, and R⁶ are asdefined above are generally prepared as described in the followingliterature references;

-   Sekikawa; Bull. Chem. Soc. Jpn. 31, (1958), 252.-   Zehra; Chem. Ber. 23, (1890), 3629.-   Palmer, B. D. et al.; J. Med. Chem. 41, (1998), 5457-5465.-   Chi, Y.-C. and Sun, C.-M.; Syn. Lett. 5, (2000), 591-594.-   Wu, Z. et al.; Tetrahedron Lett. 41, (2000), 9871-9874.

By allowing an acid (I) wherein R¹, R², R³, R⁵, and R⁶ are as definedabove to be coupled with an amine (II) wherein R⁷ and R⁸ are defined asabove under standard amide forming conditions using a coupling reagent(a) (e.g. HOBT, EDAC and DIPEA in dry THF) affording amide (III) whereinR¹, R², R³, R⁵, R⁵, R⁷ and R⁸ are as defined above.General Method B

By allowing an acid derivative (I) wherein X is halo, R⁹(C═O)O—,C₁-C₆alkyloxy or arylC₁-C₆alkyloxy, R⁹ is C₁-C₆alkyl or arylC₁-C₆alkyland R¹, R², R³, R⁵ and R⁶ are defined as above to react with an amine(II) wherein R⁷ and R⁸ are defined as above under basic conditions (e.g.triethylamine, K₂CO₃, NaH and the like) in a solvent (e.g. THF, DCM,DMF, NMP and the like) affording amide (III); wherein R¹, R², R³, R⁴,R⁵, R⁶, R⁷ and R⁸ are defined as above.

Example 1 1H-Benzoimidazole-5-carboxylic acid cyclohexyl-methyl-amide

A solution of 1H-benzoimidazole-5-carboxylic acid (10 g, 61.67 mmol) andHOBT (9.17 g, 67.84 mmol) in dry THF (250 ml) was stirred for 1 h. EDAC(13 g, 67.84 mmol) was added and the mixture was stirred for another 1h. Di-isopropyl ethyl amine (DIPEA) (11.8 ml, 67.84 mmol) andcyclohexyl-methyl-amine (8.8 ml, 67.84 mmol) was added and the resultingmixture was stirred for 16 hrs. at room temperature. The precipitate wasfiltered off and the volatiles were evaporated in vacuo. To the residuewas added water (150 ml) and diethyl ether (75 ml) and the resultingmixture was stirred for 15 minutes. The precipitate was filtered off andwashed with water followed by diethyl ether and drying in vacuo at 50°C. which afforded 7.7 g (49%) of the title compounds as a solid.

¹H NMR (300 MHz, CDCl₃) δ 1.03 (bs, 2H), 1.53-1.86 (m, 8H), 2.93 (bd,3H), 3.57 and 4.56 (2×bs, 1H), 7.19 (d, 1H), 7.44 (bs, 1H), 7.62 (s,1H), 7.79 (s, 1H), 11.8 (bs, 1H, NH).

Calculated for C₁₅H₁₉N₃O;

C, 70.01%; H, 7.44%; N, 16.33%. Found:

C, 69.63%; H, 7.45%; N, 16.17%.

The following compounds were synthesised in a similar way as describedin example 1

Example 2 Isopropyl-2-trifluoromethyl-1H-benzoimidazole-5-carboxylicacid cyclohexyl-methyl-amide

Calculated for C₁₉H₂₄F₃N₃O;

C, 62.11%; H, 6.58%; N, 11.44%. Found

C, 62.10%; H, 6.69%; N, 11.66%.

Example 3 1-Benzyl-1H-benzoimidazole-5-carboxylic acidcyclohexyl-methyl-amide

Calculated for C₂₂H₂₅N₃O;

C, 76.05%; H, 7.25%; N, 12.09%. Found

C, 75.89%; H, 7.39%; N, 12.03%.

Example 4 2-Methyl-1H-benzoimidazole-5-carboxylic acidcyclohexyl-methyl-amide

Calculated for C₁₆H₂₁N₃O; 0.1×H₂O;

C, 70.35%; H, 7.82%; N, 15.38%. Found

C, 70.09%; H, 7.78%; N, 15.41%.

Example 5 2-Hydroxymethyl-1H-benzoimidazole-5-carboxylic acidcyclohexyl-methyl-amide

Calculated for C₁₆H₂₁N₃O₂;

C, 66.88%; H, 7.37%; N, 14.62%. Found

C, 66.62%; H, 7.50%; N, 14.43%.

Example 6 2-(4-Amino-phenyl)-1H-benzoimidazole-5-carboxylic acidcyclohexyl-methyl-amide

LC/MS m/z: 349H⁺

¹H NMR (300 MHz, CDCl₃) δ 1.03-1.3 (m, 4H), 1.45-1.80 (m, 6H), 2.84 (bd,3H), 5.65 (bs, 2H), 6.66 (d, 2H), 7.12 (m, 1H), 7.48 (m, 2H), 7.84 (d,2H), 12.6 (bs, 1H, NH).

Example 7(1H-Benzoimidazol-5-yl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone

LC/MS m/z: 298H⁺

¹H NMR (400 MHz, CDCl₃) δ 0.95 (d, 3H), 1.04 (d, 3H), 1.15 (d, 3H),1.19-1.87 (m, 5.5H), 2.25 (m, 0.5H), 3.24-3.34 (m, 1.5H), 3.69 (d,0.5H), 3.99 (m, 0.5H), 4.66 (m, 0.5H), 7.60 (t, 1H), 7.84 (t, 1H), 7.94(d, 1H), 9.08 (s, 1H).

Example 8(2-Methyl-1H-benzoimidazol-5-yl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone

¹H NMR (300 MHz, CDCl₃) δ 0.93 (d, 3H), 1.02 (d, 3H), 1.15 (m, 3H),1.19-1.85 (m, 5.5H), 2.27 (m, 0.5H), 2.50 (s, 3H), 3.22-3.35 (m, 1.5H),3.64 (d, 0.5H), 4.06 (m, 0.5H), 4.64 (m, 0.5H), 7.22 (m, 2H), 7.58 (m,1H).

Example 9(2-Amino-1H-benzoimidazol-5-yl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone

LC/MS m/z: 313H⁺

¹H NMR (300 MHz, CDCl₃) δ 0.91 (d, 3H), 1.04 (d, 3H), 1.13 (s, 3H),1.2-1.82 (m, 5.5H), 2.18 (m, 0.5H), 3.22-3.26 (m, 1.5H), 3.62 (d, 0.5H),4.01 (m, 0.5H), 4.54 (m, 0.5H), 7.21 (m, 3H), 8.14 (m, 2H).

EXAMPLES Compounds of General Formula (VI)

The following examples and general procedures refer to intermediatecompounds and final products for general formula (VI) identified in thespecification and in the synthesis schemes. The preparation of thecompounds of general formula (VI) of the present invention is describedin detail using the following examples. Occasionally, the reaction maynot be applicable as described to each compound included within thedisclosed scope of the invention. The compounds for which this occurswill be readily recognised by those skilled in the art. In these casesthe reactions can be successfully performed by conventionalmodifications known to those skilled in the art, that is, by appropriateprotection of interfering groups, by changing to other conventionalreagents, or by routine modification of reaction conditions.Alternatively, other reactions disclosed herein or otherwiseconventional will be applicable to the preparation of the correspondingcompounds of the invention. In all preparative methods, all startingmaterials are known or may easily be prepared from known startingmaterials. The structures of the compounds are confirmed by eitherelemental analysis or nuclear magnetic resonance (NMR), where peaksassigned to characteristic protons in the title compounds are presentedwhere appropriate. ¹H NMR shifts (8H) are given in parts per million(ppm) down field from tetramethylsilane as internal reference standard.M.p.: is melting point and is given in ° C. and is not corrected. Columnchromatography was carried out using the technique described by W. C.Still et al., J. Org. Chem. 43: 2923 (1978) on Merck silica gel 60 (Art.9385). HPLC analyses are performed using 5 μm C18 4×250 mm column elutedwith various mixtures of water and acetonitrile, flow=1 ml/min, asdescribed in the experimental section.

The abbreviations as used in the examples have the following meaning:

TLC: thin layer chromatography

CDCl₃: deuterio chloroform

CD₃OD: tetradeuterio methanol

DMSO-d₆: hexadeuterio dimethylsulfoxide

DMSO: dimethylsulfoxide

THF: tetrahydrofuran

DMF: N,N-dimethylformamide

HOBT: 1-hydroxy-benzotriazole

EDAC: 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide, hydrochloride

min: minutes

hrs: hours

The compounds of the invention are prepared as illustrated in thefollowing reaction scheme 1:

General Method A:

By allowing a carboxylic acid ester (I) wherein R¹³ is C₁-C₆alkyl orarylC₁-C₆alkyl and R⁷ is as defined above to react with an alkene (II)wherein X is halo and R¹, R², R³, R⁴, and n are as defined above underbasic conditions using a base (K₂CO₃, TEA, DIPEA in dry acetone, MIBKand the like) affording aryl ether (III) wherein R¹, R², R³, R⁴, R⁷, R¹³and n are as defined above. Aryl ether (III) wherein R¹, R², R³, R⁴, R⁷,R¹³ and n are as defined above is rearranged in e.g. NMP at refluxtemperature into phenol (IV) wherein R¹, R², R³, R⁴, R⁷, R¹³ and n areas defined above. Treatment of phenol (IV) wherein R¹, R², R³, R⁴, R⁷,R¹³ and n are as defined above with 90% formic acid followed by basichydrolysis and acidic work up affords dihydrobenzofurane (V) wherein R¹,R², R³, R⁴, R⁷ and n are as defined above. Dihydrobenzofurane (V)wherein R¹, R², R³, R⁴, R⁷ and n are as defined above is coupled with anamine (VI) wherein R⁵ and R⁶ are defined as above under standard amideforming conditions using a coupling reagent (a) (e.g. HOBT, EDAC andDIPEA in dry THF) affording amide (VII) wherein R¹, R², R³, R⁴, R⁵, R⁶,R⁷ and n are as defined above.General Method B:

By allowing an acid derivative (I) wherein Y is halo, R¹³(C═O)O—,C₁-C₆alkyloxy or arylC₁-C₆alkyloxy, R¹³ is C₁-C₆alkyl or arylC₁-C₆alkyland R³, R⁴, R⁷ and X are defined as above to react with an amine (II)wherein R⁵ and R⁶ are defined as above under basic conditions (e.g.triethylamine, K₂CO₃, NaH and the like) in a solvent (e.g. THF, DCM,DMF, NMP and the like) affording amide (III); wherein R³, R⁴, R⁵, R⁶, R⁷and X are defined as above.

In the following “general methods C to H” is provided guidelines forsynthesis of substituted benzofuranes-,2,3-dihydrobenzofuranes-7-carboxylic acids and croman-8-carboxylic acids(compound V in scheme 1) according to literature references;General Method C:

wherein X is halo, R¹³ and R¹⁴ are independently C₁-C₆alkyl orarylC₁-C₆alkyl and R¹, R³, and R⁷ are defined as above.

-   Cherif, M.; Cotelle, P.; Catteau, J.-P.; Heterocycles (1992), 34,    1749-1758.-   Barker, P.; Finke, P.; Thompson, K.; Synth Commun (1989), (19), 257.    General Method D:    wherein X is OH or halo; R¹³ is C₁-C₆alkyl or arylC₁-C₆alkyl and R¹,    R³, and R⁷ are defined as above.-   Catalyst: AIBN: Graham, S. R.; Murphy, J. A.; Coates, D.;    Tetrahedron Lett., 40, (1999), 2415-2416.-   Catalyst: Pd(OAc)₂: Larock, R. C.; Stinn, D. E.; Tetrahedron Lett.;    29; (1988), 4687-4690.    General Method E:    wherein R′ is CN or COOR″; R¹ is hydrogen, C₁-C₆alkyl, aryl,    heteroaryl or arylC₁-C₆alkyl; R³ is aryl, heteroaryl, cyano, COR¹³,    nitro or COOR″, wherein R″ and R¹³ independently are C₁-C₆alkyl,    aryl, heteroaryl, or arylC₁-C₆alkyl;-   Lau, C. K. et al.; J. Med. Chem. 32, (1989) 1190-1197.    For conversion of R′═CN to COOH see e.g. Cagniant; Bull. Soc. Chim.    Fr.; (1957), 827-834.    General Method F:    wherein R′ is hydrogen or bromo; R¹, R³ and R⁷ are defined as above;-   Al-bojuk, N. R.; El-Abadelah, M. M.; Sabri, S. S.; Michel, A.;    Voelter, W.; M.-Moessmer, C.; Al-Abed, Y.; Heterocycles; 55, (2001),    1789-1804.-   Stanetty, P.; Koller, H.; Puerstinger, G.; Monatsh. Chem., 121,    (1990), 883-891.    General Method H:    wherein R¹³ is C₁-C₆alkyl, aryl, heteroaryl, or arylC₁-C₆alkyl and    R¹, R² and R⁷ are defined as above;-   Kakigami, T.; Baba, K.; Usui, T.; Heterocycles; 48, (1998),    2611-2620.

Example 1 General Method B2,3-Dimethyl-2,3-dihydro-benzofuran-7-carboxylic acidcyclohexyl-methyl-amide

To a solution of 2,3-dimethyl-2,3-dihydro-benzofuran-7-carboxylic acid(0.5 g, 2.60 mmol), HOBT (0.39 g, 2.86 mmol) in dry THF (25 ml) wasadded EDAC (0.55 g, 2.86 mmol). The mixture was stirred for 10 min.followed by addition of di-isopropyl ethyl amine (DIPEA) (0.5 ml, 2.86mmol) and cyclohexyl-methyl-amine (0.37 ml, 2.86 mmol). The resultingmixture was stirred for 16 hrs. at room temperature, the volatiles wereevaporated in vacuo and to the residue was added water (25 ml) anddiethyl ether (75 ml). The organic phase was separated and dried(Na₂SO₄), filtered and the solvent evaporated in vacuo. The residue wasdissolved in a mixture of AcOEt/Heptane (1:1) and filtered through a 2.5cm silicagel plug. The solvent was evaporated in vacuo affording 0.7 g(93%) of the title compounds as an oil.

¹H NMR (300 MHz, CDCl₃) δ 1.06 (m, 3H), 1.29 (m, 4H), 1.48 (m, 5H),1.67-1.8 (m, 4H), 2.77 and 2.97 (d and s, 3H, rotamer), 3.05 and 4.37(2×m, 1H), 3.35 and 4.55 (2×m, 1H), 3.39 and 4.89 (2×m, 1H), 6.86 (t,1H), 7.12 (t, 2H).

Calculated for C₁₈H₂₅NO₂, 0.15H₂O

C, 74.52%; H, 8.79%; N, 4.83%. Found:

C, 74.54%; H, 8.98%; N, 4.98%.

The following compounds were synthesised in a similar way as describedin Example 1 (general method B). No. Structure MW lupac Name B-1

259.35 2,3-Dihydro-benzofuran-7-carboxylic acid cyclo-hexyl-methyl-amide B-2

257.34 Benzofuran-7-carboxylic acid cyclohexyl-methyl- amide B-3

273.38 2-Methyl-2,3-dihydro-benzofuran-7-carboxylic acidcyclohexyl-methyl-amide B-4

271.36 2-Methyl-benzofuran-7-carboxylic acid cyclohexyl- methyl-amideB-5

287.41 3,3-Dimethyl-2,3-dihydro-benzofuran-7-carboxylic acidcyclohexyl-methyl-amide B-6

327.47 (2,3-Dimethyl-2,3-dihydro-benzofuran-7-yl)-(2,4,4-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone B-7

303.40 4-Methoxy-2-methyl-2,3-dihydro-benzofuran-7- carboxylic acidcyclohexyl-methyl-amide B-8

287.41 2,2-Dimethyl-2,3-dihydro-benzofuran-7-carboxylic acidcyclohexyl-methyl-amide B-9

313.44 (2-Methyl-2,3-dihydro-benzofuran-7-yl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone B-10

273.37 Chroman-8-carboxylic acid cyclohexyl-methyl- amide

EXAMPLES Compounds of General Formula (VII)

The following examples and general procedures refer to intermediatecompounds and final products for general formula (VII) identified in thespecification and in the synthesis schemes. The preparation of thecompounds of general formula (VII) of the present invention is describedin detail using the following examples. Occasionally, the reaction maynot be applicable as described to each compound included within thedisclosed scope of the invention. The compounds for which this occurswill be readily recognised by those skilled in the art. In these casesthe reactions can be successfully performed by conventionalmodifications known to those skilled in the art, that is, by appropriateprotection of interfering groups, by changing to other conventionalreagents, or by routine modification of reaction conditions.Alternatively, other reactions disclosed herein or otherwiseconventional will be applicable to the preparation of the correspondingcompounds of the invention. In all preparative methods, all startingmaterials are known or may easily be prepared from known startingmaterials. The structures of the compounds are confirmed by nuclearmagnetic resonance (NMR), where peaks assigned to characteristic protonsin the title compounds are presented where appropriate. ¹H NMR shifts(δ._(H)) are given in parts per million (ppm) down field fromtetramethylsilane as internal reference standard. M.p.: is melting pointand is given in ° C. and is not corrected. Column chromatography wascarried out using the technique described by W. C. Still et al., J. Org.Chem. 43: 2923 (1978) on Merck silica gel 60 (Art. 9385). LC-MS analysesare performed using Waters XTerra MS C-3×18 mm RP-C18 column eluted withvarious mixtures of water and acetonitrile, flow=1 mL/min, with UVdetection at 210 nm and MS scanning (ES+) from 100-1000 amu. Aninjection volume of 1 μL was used.

Microwave oven synthesis: The reaction was heated by microwaveirradiation in sealed microwave vessels in a single mode Emrys OptimizerEXP from PersonalChemistry®.

Solid-phase synthesis: All reactions were performed in Teflon apparatussuitable for solid-phase synthesis or on an ACT 496 robot employing thestandard procedures described.

Preparative HPLC: Column: 1.9×15 cm Waters XTerra RP-18. Buffer: lineargradient 5-95% in 15 min, MeCN, 0.1% TFA, flow rate of 15 mL/min. Thepooled fractions are either evaporated to dryness in vacuo, orevaporated in vacuo until the MeCN is removed, and then frozen andfreeze dried.

The abbreviations as used in the examples have the following meaning:

TLC: Thin layer chromatography

CDCl₃: Deuterio chloroform

CD₃OD: Tetradeuterio methanol

DMSO-d₆: Hexadeuterio dimethylsulfoxide

DMSO: Dimethylsulfoxide

THF: Tetrahydrofuran

DMF: N,N-dimethylformamide

HOBT: 1-Hydroxy-benzotriazole

EDAC: 1-(3-Ddimethylaminopropyl)-3-ethylcarbodiimide, hydrochloride

min: minutes

hrs: hours

The compounds of the invention are prepared as illustrated in thefollowing reaction schemes:General Method A

Indole-7-carboxylic acids (I) wherein R¹, R³, R⁴, R⁵ and R⁶ are asdefined above are generally prepared as described in the followingliterature references;

-   Clark, R. D. et al.; J. Heterocycl. Chem. 22, (1985), 121-125.-   Kasahara, A. et al.; J. Heterocycl. Chem. 26, (1989), 1405-1413.-   Kamiya, S. et al.; Chem. Pharm. Bull. 43, (1995), 1692-1695.-   Somei, M. et al.; Chem. Pharm. Bull. 34, (1986), 4116-4125.-   Wiedenau, P. et al.; Synth. Commun. 27, (1997), 2033-2040.-   Soederberg, B. C. et al.; J. Org. Chem. 62, (1997), 5838-5845.

By allowing an acid (I) wherein R¹, R³, R⁴, R⁵ and R⁶ are as definedabove to be coupled with an amine (II) wherein R⁷ and R⁸ are defined asabove under standard amide forming conditions using a coupling reagent(a) (e.g. HOBT, EDAC and DIPEA in dry DMF) affording amide (III) whereinR¹, R³, R⁴, R⁵, R⁶, R⁷ and R⁸ are as defined above.General Method B

Indole-6-carboxylic acids (I) wherein R¹, R², R⁴, R⁵ and R⁶ are asdefined above are generally prepared as described in the followingliterature references;

-   Kermack; J. Chem. Soc. 125, (1924), 2288.-   Tischler, A. N.; Lanza, T. J.; Tetrahedron Lett. 27, (1986),    1653-1656.-   Gharagozloo, P. et al.; Tetrahedron, 52, (1996), 10185-10192.-   Zhang, H.-C. et al.; Tetrahedron Lett. 39, (1998), 4449-4452.-   Kasahara, A. et al.; J. Heterocycl. Chem. 24, (1987), 1555-1556.-   Brown, F. J. et al.; J. Med. Chem. 35, (1992), 2419-2439.-   Izumi, T. et al.; J. Heterocycl. Chem. 29, (1992), 1625-1629.-   Soederberg, B. C and Shriver, J. A.; J. Org. Chem. 62, (1997),    5838-5845.-   Kitano, M. et al.; Chem. Pharm. Bull. 47, (1999), 1538-1548.-   Snyder et al.; J. Am. Chem. Soc. 80, (1958), 4622-4624.

By allowing an acid (I) wherein R¹, R², R⁴, R⁵ and R⁶ are as definedabove to be coupled with an amine (II) wherein R⁷ and R⁸ are defined asabove under standard amide forming conditions using a coupling reagent(a) (e.g. HOBT, EDAC and DIPEA in dry DMF) affording amide (III) whereinR¹, R², R⁴, R⁵, R⁶, R⁷ and R⁸ are as defined above.General Method C

Indole-5-carboxylic acids (I) wherein R¹, R², R³, R⁵ and R⁶ are asdefined above are generally prepared as described in the followingliterature references;

-   Singer, S., J. Org. Chem. 20, (1955), 1458.-   Noland, W. E. and Reich, C.; J. Org. Chem. 32, (1967), 828-832.-   Street, L. J. et al.; J. Med. Chem. 36, (1993), 1529-1538.-   Bosch, J. et al.; Tetrahedron, 57, (2001), 1041-1048.-   Agarwal, A. et al.; J. Med. Chem. 36, (1993), 4006-4014.-   Kasahara, A. et al.; J. Heterocycl. Chem. 26, (1989); 1405-1413.-   Boettcher, H. and Gericke, R.; Liebigs Ann. Chem. (1988), 749-752.-   Somei, M. et al.; Chem. Pharm. Bull. 34, (1986), 4116-4125.-   Kamiya, S. et al.; Chem. Pharm. Bull. 43, (1995), 1692-1695.-   Odle, R. et al.; J. Org. Chem. 45, (1980), 2709-2710.

By allowing an acid (I) wherein R¹, R², R³, R⁵ and R⁶ are as definedabove to be coupled with an amine (II) wherein R⁷ and R⁸ are defined asabove under standard amide forming conditions using a coupling reagent(a) (e.g. HOBT, EDAC and DIPEA in dry DMF) affording amide (III) whereinR¹, R², R³, R⁵, R⁶, R⁷ and R⁸ are as defined above.General Method D

Indole-4-carboxylic acids (I) wherein R¹, R², R³, R⁴ and R⁶ are asdefined above are generally prepared as described in the followingliterature references;

-   Beswick, P. J. et al.; Tetrahedron 44, (1988), 7325.-   Muchowski, J. M. et al.; Tetrahedron Lett. 28, (1987), 3453.-   Kasahara, A. et al.; J. Heterocycl. Chem. 26, (1989); 1405-1413.-   Kasahara, A. et al.; J. Heterocycl. Chem. 24, (1987), 1555-1556.-   Clark, R. D. et al.; J. Heterocycl. Chem. 22, (1985), 121-125.-   Kruse, L. I. Heterocycles, 16, (1981), 1119-1124.-   Soederberg, B. C. Org. Synth. 80, (2002), 75.

By allowing an acid (I) wherein R¹, R², R³, R⁴ and R⁶ are as definedabove to be coupled with an amine (II) wherein R⁷ and R⁸ are defined asabove under standard amide forming conditions using a coupling reagent(a) (e.g. HOBT, EDAC and DIPEA in dry DMF) affording amide (III) whereinR¹, R², R³, R⁴, R⁶, R⁷ and R⁸ are as defined above.General Method E

Indole-3-carboxylic acids (I) wherein R¹, R², R³, R⁴ and R⁵ are asdefined above are generally prepared as described in the followingliterature references;

-   Weissgerber; Chem. Ber. 43, (1910), 3526.-   Whalley; J. Chem. Soc. (1954), 1651.-   Bravo, P. et al.; Tetrahedron Lett. 10, (1969), 679.-   Sus, O. et al.; Justus Liebigs Ann. Chem. (1953), 583, 150.-   Melzer, M. S. et al.; J. Org. Chem. 27, (1962), 496.-   Amat, M. et al.; J. Org. Chem. 59, (1994), 10-11.

By allowing an acid (I) wherein R¹, R², R³, R⁴ and R⁵ are as definedabove to be coupled with an amine (II) wherein R⁷ and R³ are defined asabove under standard amide forming conditions using a coupling reagent(a) (e.g. HOBT, EDAC and DIPEA in dry DMF) affording amide (III) whereinR¹, R², R³, R⁴, R⁵, R⁷ and R⁸ are as defined above.

Example 1(1H-Indol-5-yl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone

A solution of 1H-indole-5-carboxylic acid (1.0 g, 6.21 mmol), HOBT (0.9g, 6.83 mmol) in dry THF (50 mL) and EDAC (1.31 g, 6.83 mmol) wasstirred for 10 mins. Di-isopropyl ethyl amine (DIPEA) (1.2 mL, 6.83mmol) and 6-aza-bicyclo[3.2.1]octyl)-amine (1.16 mL, 6.83 mmol) wasadded and the resulting mixture was stirred for 16 hrs. at roomtemperature. The volatiles were evaporated in vacuo and to the residuewas added water (25 mL) followed by extraction with diethyl ether (2×25mL). The combined organic phases were dried (Na₂SO₄), filtered andevaporated in vacuo. The residue was purified by silicagelchromatography using a mixture of ethyl acetate and heptane (1:2) aseluent. Pure fractions were collected and the solvent evaporated invacuo. To the residue was added diethyl ether (10 mL) and the resultingmixture was stirred for 1 h. The precipitate was filtered off and driedin vacuo at 50° C. affording 1.3 g (71%) of the title compounds as asolid.

MS-ESI m/z 297; ¹H NMR (300 MHz, CDCl₃) δ 0.93-1.44 (m, 13H), 1.62 (m,1H), 1.76 (m, 1H), 2.29 and 3.28 (2×m, 1H), 3.31 and 3.62 (2×m, 1H),4.10 and 4.65 (2×m, 1H), 6.59 (s, 1H), 7.22-7.35 (m, 3H), 7.74 (d, 1H),8.69 (bs, 1H, NH).

Example 2 1H-Indole-6-carboxylic acid cyclohexyl-methyl-amide

A solution of 1H-indole-6-carboxylic acid (1.0 g, 6.21 mmol), HOBT (0.92g, 6.83 mmol) in dry THF (50 mL) and EDAC (1.31 g, 6.83 mmol) wasstirred for 20 mins. Di-isopropyl ethyl amine (DIPEA) (1.2 mL, 6.83mmol) and cyclohexyl-methyl-amine (0.9 mL, 6.83 mmol) was added and theresulting mixture was stirred for 16 hrs. at room temperature. To theprecipitate was added water (50 mL), the solid filtered off, washed withwater followed by diethyl ether and dried in vacuo at 50° C. whichafforded 0.6 g (38%) of the title compounds as a solid.

¹H NMR (300 MHz, CDCl₃) δ 1.05 (bm, 2H), 1.15-1.85 (m, 8H), 2.96 (bs,3H), 3.65 and 4.55 (2×m, 1H), 6.54 (s, 1H), 7.09 (d, 1H), 7.24 (m, 1H),7.50 (s, 1H), 7.60 (d, 1H), 8.89 (bs, 1H, NH).

Calculated for C₁₆H₂₀N₂O;

C, 74.97%; H, 7.86%; N, 10.93%. Found: C, 74.90%; H, 8.01%; N, 10.88%.

Example 3(1H-Indol-7-yl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone

A solution of 1H-indole-7-carboxylic acid (323 mg, 2 mmol), HOAt (300mg, 2.2 mmol) in dry DMF (10 mL) and EDAC (500 mg, 2.6 mmol) was stirredfor 10 mins. Triethylamine (TEA) (0.84 mL, 6 mmol) and6-aza-bicyclo[3.2.1]octyl)-amine (338 mg, 2.2 mmol) was added and theresulting mixture was stirred for 16 hrs. at room temperature. Thevolatiles were evaporated in vacuo and to the residue was added water(10 mL) followed by extraction with dichloromethane (DCM, 2×25 mL). Thecombined organic phases were dried (MgSO₄), filtered and evaporated invacuo. The residue was purified by preparative HPLC, dried in vacuo at50° C. affording 283 mg (47%) of the title compound as a solid.

MS-ESI m/z 297; ¹H NMR (300 MHz, DMSO) δ 0.85-1.40 (m, 13H), 1.50-1.54(m, 1H), 1.80-1.86 (m, 1H), 2.19-2.24 and 2.43-2.57 (2×m, 1H), 3.13 and3.32 (m, 1H), 3.84-3.87 and 4.47-4.50 (2×m, 1H), 6.46-6.49 (m, 1H),7.00-7.19 (m, 2H), 7.30-7.34 (m, 1H), 7.60-7.63 (m, 1H), 10.97 (d, 1H,NH).

Example 4(1H-Indol-6-yl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone

A solution of 1H-indole-6-carboxylic acid (1 g, 6.2 mmol), HOAt (929 mg,6.82 mmol) in dry DMF (20 mL) and EDAC (1.54 g, 8.06 mmol) was stirredfor 10 mins. TEA (2.59 mL, 18.6 mmol) and6-aza-bicyclo[3.2.1]octyl)-amine (1.04 g, 6.82 mmol) was added and theresulting mixture was stirred for 5 hrs. at room temperature. Thevolatiles were evaporated in vacuo and to the residue was added water(10 mL) followed by extraction with dichloromethane (DCM, 2×50 mL). Thecombined organic phases were dried (MgSO₄), filtered and evaporated invacuo. The residue was purified by silicagel chromatography using amixture of ethyl acetate and heptane (3:7) as eluent. Pure fractionswere collected, the solvent evaporated in vacuo and dried in vacuo at50° C. affording 1.6 g (87%) of the title compounds as a solid.

MS-ESI m/z 297; ¹H NMR (300 MHz, CDCl₃) δ 0.93 (d, 3H), 1.02 (d, 3H),1.11-1.15 (m, 4H), 1.26-1.39 (m, 2H), 1.56-1.66 (m, 1H), 1.73-1.79 and2.27-2.33 (2×m, 2H), 3.22-3.35 and 3.61-3.65 (m, 2H), 4.07-4.10 and4.62-4.65 (2×m, 1H), 6.52-6.54 (m, 1H), 7.17-7.25 (m, 2H), 7.53-7.63 (m,2H), 9.03 (bs, 1H, NH).

The following compounds were synthesised employing a similar method tothe ones described in examples 1, 2, 3 and 4 above: MS-ESI No MoleculeMW IUPAC Name m/z 4-1

294.40 1H-Indole-6-carboxylic acid adamantan-2-ylamide 295 4-2

254.33 (6-Aza-bicyclo[3.2.1]oct-6-yl)- (1H-indol-6-yl)-methanone 255 4-3

283.37 1H-Indole-6-carboxylic acid (8- methyl-8-aza-bicyclo[3.2.1]oct-3-yl)-amide 284 4-4

294.40 1H-Indole-5-carboxylic acid adamantan-2-ylamide 295 4-5

254.33 (6-Aza-bicyclo[3.2.1]oct-6-yl)- (1H-indol-5-yl)-methanone 255 4-6

296.40 (1H-Indol-4-yl)-(1,3,3-trimethyl- 6-aza-bicyclo[3.2.1]oct-6-yl)-methanone 297 4-7

296.40 (1H-Indol-3-yl)-(1,3,3-trimethyl- 6-aza-bicyclo[3.2.1]oct-6-yl)-methanone 297 4-8

296.40 (1H-Indol-2-yl)-(1,3,3-trimethyl- 6-aza-bicyclo[3.2.1]oct-6-yl)-methanone 297 4-9

310.44 (1-Methyl-1H-indol-3-yl)-(1,3,3- trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)- methanone 311 4-10

268.36 (3-Aza-bicyclo[3.2.2]non-3-yl)- (1H-indol-3-yl)-methanone 2694-11

270.38 1-Methyl-1H-indole-3- carboxylic acid cycloheptyl- amide 271 4-12

308.42 1-Methyl-1H-indole-3- carboxylic acid adamantan-1- ylamide 3094-13

282.39 (3-Aza-bicyclo[3.2.2]non-3-yl)- (1-methyl-1H-indol-3-yl)-methanone 283 4-14

257.34 (1-Methyl-1H-indol-3-yl)-(4- methyl-piperazin-1-yl)- methanone258 4-15

324.43 1-Methyl-1H-indole-3- carboxylic acid (3-hydroxy-adamantan-1-yl)-amide 325 4-16

324.42 1-Methyl-1H-indole-3- carboxylic acid azepan-1- ylamide 325 4-17

285.35 1-Methyl-1H-indole-3- carboxylic acid (2-oxo-azepan- 3-yl)-amide286 4-18

332.45 (4-Benzyl-piperidine-1-yl)-(1- methyl-1H-indol-3-yl)- methanone333 4-19

285.39 1-Methyl-1H-indole-3- carboxylic acid (2,6-dimethyl-piperidin-1-yl)-amide 286 4-20

256.35 1-Methyl-1H-indole-3- carboxylic acid (2-methyl-piperidin-1-yl)-amide 257 4-21

368.50 (1-Cyclopropylmethyl-6-fluoro- 1H-indol-3-yl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)- methanone 369 4-22

256.35 Azepan-1-yl-(1-methyl-1H- indol-3-yl)methanone 257 4-23

402.54 (5-Benzyloxy-1H-indol-3-yl)- (1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)- methanone 403 4-24

340.42 (5H-[1,3]Dioxolo[4,5]indol-7- yl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)- methanone 341 4-25

330.86 (5-Chloro-1H-indol-3-yl)-(1,3,3- trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)- methanone 332 4-26

364.41 (6-Trifluoromethyl-1H-indol-3- yl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)- methanone 365 4-27

310.44 (6-Methyl-1H-indol-3-yl)-(1,3,3- trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)- methanone 311 4-28

341.41 (6-Nitro-1H-indol-3-yl)-(1,3,3- trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)- methanone 342 4-29

326.44 (5-Methoxy-1H-indol-3-yl)- (1,3,3-trimethyl-6-aza-bicyclo[3.2.1]cct-6-yl)- methanone 327 4-30

314.40 (6-Fluoro-1H-indol-3-yl)-(1,3,3- trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)- methanone 315 4-31

326.44 (6-Methoxy-1H-indol-3-yl)- (1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)- methanone 327 4-32

341.41 (7-Nitro-1H-indol-3-yl)-(1,3,3- trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)- methanone 342 4-33

296.40 (1H-Indol-4-yl)-(1,3,3-trimethyl- 6-aza-bicyclo[3.2.1]oct-6-yl)-methanone 297 4-34

310.44 2-(1H-Indol-3-yl)-1-(1,3,3- trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)- ethanone 311 4-35

282.39 1-(3-Aza-bicyclo[3.2.2]non- 3-yl)-2-(1H-indol-3-yl)- ethanone 2834-36

296.42 1-(3-Aza-bicyclo[3.2.2]non- 3-yl)-2-(1-methyl-1H-indol-3-yl)-ethanone 297 4-37

324.47 2-(1-Methyl-1H-indol-3-yl)-1- (1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)- ethanone 325 4-38

426.55 [3-(1,3,3-Trimethyl-6-aza- bicyclo[3.2.1]octane-6-carbonyl)-1H-indol-6-yloxy]- acetic acid tert-butyl ester 427

Example 56-(1,3,3-Trimethyl-6-aza-bicyclo[3.2.1]octane-6-carbonyl)-1H-indole-3-carboxylicacid

To a solution of(1H-Indol-6-yl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone(1.49 g, 5.02 mmol) in pyridine (0.81 mL, 5.02 mmol) and DCM (25 mL) at0° C. was added trichloroacetyl chloride after which cooling was stoppedand the resulting mixture was stirred for 16 hrs. at room temperature.The volatiles were evaporated in vacuo and to the residue was addedwater (20 mL) followed by extraction with dichloromethane (DCM, 2×50mL). The combined organic phases were dried (MgSO₄), filtered andevaporated in vacuo to afford 2.48 g (100%) of2,2,2-Trichloro-1-[6-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]octane-6-carbonyl)-1H-indol-3-yl]-ethanone.To2,2,2-Trichloro-1-[6-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]octane-6-carbonyl)-1H-indol-3-yl]-ethanone(100 mg, 0.22 mmol) was added a solution of ethanol:THF:1M NaOH solution(20 mL, 1:2:1, v/v/v) and the mixture was stirred at room temperaturefor 5 hrs. The organic solvents were evapourated in vacuo and theaqueous collections were acidified to pH 1 with concentratedhydrochloric acid followed by extraction with ethyl acetate (2×20 mL).The combined organic phases were dried (MgSO₄), filtered, evapouratedand the residue after trituration with diethyl ether was filtered anddried in vacuo at 50° C. affording 56 mg (72%) of the title compound asa solid.

MS-ESI m/z 341; ¹H NMR (300 MHz, DMSO) δ 0.91 (d, 3H), 0.97 (d, 3H),1.09 (s, 3H), 1.13-1.54 (m, 4H), 1.73-1.78 (m, 1H), 3.13-3.18 (m, 1H),3.30-3.47 (m, 2H), 3.98-4.02 and 4.38-4.42 (2×m, 1H), 7.19-7.28 (m, 1H),7.53 (d, 1H), 7.99-8.04 (m, 1H), 8.09 (d, 1H), 11.92 (bs, 1H, NH), 12.05(bs, 1H, OH).

Example 66-(1,3,3-Trimethyl-6-aza-bicyclo[3.2.1]octane-6-carbonyl)-1H-indole-3-carboxylicacid ethyl ester

To a solution of2,2,2-Trichloro-1-[6-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]octane-6-carbonyl)-1H-indol-3-yl]-ethanone(100 mg, 0.22 mmol) in ethanol (2 mL) was added sodium ethoxide (77 mg,1.13 mmol) and the resulting mixture was stirred for 16 hrs. at roomtemperature. The volatiles were evaporated in vacuo and the residue waspurified by preparative HPLC, dried in vacuo at 50° C. affording 33 mg(43%) of the title compound as a solid.

MS-ESI m/z 369; ¹H NMR (300 MHz, CDCl₃) δ 0.91-1.01 (m, 3H), 1.12 (d,3H), 1.17-1.36 (m, 1H), 1.40-1.44 (m, 4H), 1.56-1.61 (m, 1H), 1.73-1.78(m, 1H), 3.20-3.33 and 3.62-3.66 (m, 2H), 4.05-4.08 and 4.58-4.61 (m,1H), 4.38 (q, 2H), 7.29-7.33 (m, 1H), 7.55 (d, 1H), 7.97-7.99 (m, 1H),8.15-8.19 (m, 1H), 10.01 (d, 1H, NH).

The following compounds were synthesised employing a similar method tothe ones described in examples 5 and 6. MS-ESI No Molecule MW IUPAC Namem/z 6-1

340.42 5-(1,3,3-Trimethyl-6-aza- bicyclo[3.2.1]octane-6-carbonyl)-1H-indole-3- carboxylic acid 341 6-2

368.47 5-(1,3,3-Trimethyl-6-aza- bicyclo[3.2.1]octane-6-carbonyl)-1H-indole-3- carboxylic acid ethyl ester 369 6-3

340.42 4-(1,3,3-Trimethyl-6-aza- bicyclo[3.2.1]octane-6-carbonyl)-1H-indole-3- carboxylic acid 341 6-4

368.47 4-(1,3,3-Trimethyl-6-aza- bicyclo[3.2.1]octane-6-carbonyl)-1H-indole-3- carboxylic acid ethyl ester 369

Example 7[3-(Piperidine-1-carbonyl)-1H-indol-5-yl]-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone

To 4-hydroxy-2,3,5,6-tetrafluorobenzamidomethyl polystyrene (PS-TFPresin, 100 mg, 1 mmol/g, 100-200 mesh, polystyrene-divinylbenzene 1%,Argonaut technologies, USA) pre-swollen in DCM was added a solution of5-(1,3,3-Trimethyl-6-aza-bicyclo[3.2.1]octane-6-carbonyl)-1H-indole-3-carboxylicacid (51 mg, 0.15 mmol) in DMF (0.25 mL) followed by a solution of DMAP(7.3 mg, 0.06 mmol) in DCM (0.75 mL). The mixture was shaken for 10 minbefore a solution of N,N′-diisopropylcarbodiimide (DIC, 56 mg, 0.44mmol) in DCM (0.25 mL) was added and the resulting mixture shaken for 16hrs. at room temperature. The excess solvents were removed by filtrationand the resin was washed with DMF (3×1 mL) and DCM (10×1 mL). To theresin was added a solution of piperidine (7.3 mg, 0.085 mmol) in1,2-dichloroethane (1.2 mL) and DIPEA (0.03 mL, 0.17 mmol). Theresulting mixture was shaken for 16 hrs. at room temperature. Theproduct was removed by filtration and the resin washed with DCM:MeOH (1mL, 3:1, v/v). The volatiles were evaporated in vacuo and the residuewas purified by preparative HPLC, dried in vacuo at 50° C. affording 22mg (54%) of the title compound as a solid.

MS-ESI m/z 408; ¹H NMR (300 MHz, CDCl₃) δ 0.94 (d, 3H), 1.02 (d, 3H),1.14 (s, 3H), 1.15-1.19 (m, 1H), 1.34-1.46 (m, 3H), 1.58-1.69 (m, 7H),1.78-1.83 (m, 1H), 2.25-2.31 and 3.27-3.29 (2×m, 1H), 3.33-3.34 (m, 1H),3.64-3.67 (m, 4H), 4.08-4.11 and 4.62-4.64 (2×m, 1H), 7.25-7.28 (m, 1H),7.32-7.37 (m, 1H), 7.47-7.49 (m, 1H), 7.69-7.71 (m, 1H), 9.65 (bd, 1H,NH).

The following compounds were synthesised employing a similar method tothe ones described in example 7. MS-ESI No Molecule MW IUPAC Name m/z7-1

378.48 5-(1,3,3-Trimethyl-6-aza- bicyclo[3.2.1]octane-6-carbonyl)-1H-indole-3- carboxylic acid cyanomethyl-amide 379 7-2

429.57 5-(1,3,3-Trimethyl-6-aza- bicyclo[3.2.1]octane-6-carbonyl)-1H-indole-3- carboxylic acid benzylamide 430 7-3

367.50 5-(1,3,3-Trimethyl-6-aza- bicyclo[3.2.1]ootane-6-carbonyl)-1H-indole-3- carboxylic acid dimethyl- amide 368 7-4

379.51 5-(1,3,3-Trimethyl-6-aza- bicyclo[3.2.1]octane-6-carbonyl)-1H-indole-3- carboxylic acid allylamide 380 7-5

424.59 5-(1,3,3-Trimethyl-6-aza- bicyclo[3.2.1]octane-6-carbonyl)-1H-indole-3- carboxylic acid (2- dimethylamino-ethyl)-methyl-amide 425 7-6

397.52 5-(1,3,3-Trimethyl-6-aza- bicyclo[3.2.1]octane-6-carbonyl)-1H-indole-3- carboxylic acid (2-methoxy- ethyl)-amide 398 7-7

459.59 5-(1,3,3-Trimethyl-6-aza- bicyclo[3.2.1]octane-6-carbonyl)-1H-indole-3- carboxylic acid 4-methoxy- benzylamide 460 7-8

423.56 5-(1,3,3-Trimethyl-6-aza- bicyclo[3.2.1]octane-6-carbonyl)-1H-indole-3- carboxylic acid (tetrahydro-furan-2-ylmethyl)-amide 424 7-9

437.59 [3-(2-Methoxymethyl- pyrrolidine-1-carbonyl)-1H-indol-5-yl]-(1,3,3-trimethyl-6- aza-bicyclo[3.2.1]oct-6-yl)- methanone438 7-10

437.59 [3-(2,6-Dimethyl- morpholine-4-carbonyl)-1H-indol-5-yl]-(1,3,3-trimethyl-6- aza-bicyclo[3.2.1]oct-6-yl)- methanone438 7-11

457.60 5-(1,3,3-Trimethyl-6-aza- bicyclo[3.2.1]octane-6-carbonyl)-1H-indole-3- carboxylic acid (1,1-dioxo-tetrahydro-thiophen-3-yl)- amide 458 7-12

479.67 5-(1,3,3-Trimethyl-6-aza- bicyclo[3.2.1]octane-6-carbonyl)-1H-indole-3- carboxylic acid [3-(4-methyl-piperazin-1-yl)-propyl]- amide 481 7-13

497.57 5-(1,3,3-Trimethyl-6-aza- bicyclo[3.2.1]octane-6-carbonyl)-1H-indole-3- carboxylic acid 4- trifluoromethyl-benzylamide498 7-14

419.53 5-(1,3,3-Trimethyl-6-aza- bicyclo[3.2.1]octane-6-carbonyl)-1H-indole-3- carboxylic acid (furan-2- ylmethyl)-amide 4207-15

486.62 [3-(2,3,5,6-Tetrahydro- [1,2′]bipyrazinyl-4-carbonyl)-1H-indol-5-yl]-(1,3,3- trimethyl-6-aza- bicyclo[3.2.1]oct-6-yl)-methanone 487 7-16

421.51 5-(1,3,3-Trimethyl-6-aza- bicyclo[3.2.1]octane-6-carbonyl)-1H-indole-3- carboxylic acid (2H-tetrazol- 5-ylmethyl)-amide422 7-17

475.68 [3-(1,3,3-Trimethyl-6-aza- bicyclo[3.2.1]octane-6-carbonyl)-1H-indol-5-yl]- (1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)- methanone 476 7-18

439.56 3-{[5-(1,3,3-Trimethyl-6-aza- bicyclo[3.2.1]octane-6-carbonyl)-1H-indole-3- carbonyl]-amino}-propionic acid ethyl ester 4407-19

445.57 5-(1,3,3-Trimethyl-6-aza- bicyclo[3.2.1]octane-6-carbonyl)-1H-indole-3- carboxylic acid (4-methoxy- phenyl)-amide 4467-20

411.51 3-{[5-(1,3,3-Trimethyl-6-aza- bicyclo[3.2.1]octane-6-carbonyl)-1H-indole-3- carbonyl]-amino}-propionic acid 412 7-21

242.32 Azepan-1-yl-(1H-indol-5-yl)- methanone 243 7-22

340.43 1H-Indole-5-carboxylic acid dibenzylamide 341 7-23

268.36 (3-Aza-bicyclo[3.2.2]non-3- yl)-(1H-indol-5-yl)- methanone 2697-24

318.42 (4-Benzyl-piperidin-1-yl)- (1H-indol-5-yl)-methanone 319 7-25

374.45 8-(1H-Indole-5-carbonyl)-1- phenyl-1,3,8-triaza-spiro[4.5]decan-4-one 375 7-26

354.84 [4-(4-Chloro-phenyl)-4- hydroxy-piperidin-1-yl]-(1H-indol-5-yl)-methanone 356 7-27

360.42 1-[1-(1H-Indole-5-carbonyl)- piperidin-4-yl]-1,3-dihydro-benzoimidazol-2-one 361 7-28

284.40 (4-tert-Butyl-piperidin-1-yl)- (1H-indol-5-yl)-methanone 285 7-29

329.41 1-(1H-Indole-5-carbonyl)-4- phenyl-piperidine-4- carbonitrile 3307-30

304.40 (1H-Indol-5-yl)-(4-phenyl- piperidin-1-yl)-methanone 305 7-31

331.42 (5-Benzyl-2,5-diaza- bicyclo[2.2.1]hept-2-yl)-(1H-indol-5-yl)-methanone 332 7-32

297.40 (1H-Indol-5-yl)-(4-pyrrolidin- 1-yl-piperidin-1-yl)- methanone298 7-33

314.43 1H-Indole-5-carboxylic acid (5-hydroxy-1,3,3-trimethyl-cyclohexylmethyl)-amide 315 7-34

330.43 1H-Indole-5carboxylic acid (3,4-dihydrospiro(1H-indene-1,4-piperidine)- amide 331

Example 8(3-Methanesulfonylmethyl-1H-indol-5-yl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone

A solution of(1H-Indol-5-yl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone(300 mg, 1.01 mmol), paraformaldehyde (35 mg, 1.16 mmol), sodiummethylsulfonate (103 mg, 1.01 mmol) and acetic acid (0.1 mL) in DMF (2mL) was heated at 90° C. for 3 hrs. After cooling, the mixture waspoured onto water (100 mL) followed by extraction with DCM (3×50 mL).The combined organic phases were dried (MgSO₄), filtered and evaporatedin vacuo. The residue was purified by preparative HPLC, dried in vacuoat 50° C. affording 167 mg (43%) of the title compound as a solid.

MS-ESI m/z 389; ¹H NMR (300 MHz, CDCl₃) δ 0.94 (d, 3H), 1.03 (d, 3H),1.14-1.17 (m, 4H), 1.29-1.40 (m, 2H), 1.57-1.62 (m, 1H), 1.79-1.84 (m,1H), 2.67 (d, 3H), 3.25-3.34 and 3.64-3.67 (2×m, 2H), 4.08-4.11 and4.61-4.64 (2×m, 1H), 4.39 (s, 2H), 7.22-7.32 (m, 3H), 7.78 (d, 1H), 9.42(s, 1H, NH).

Example 9(3-Dimethylaminomethyl-1H-indol-6-yl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone

To a solution of(1H-Indol-6-yl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone(200 mg, 0.67 mmol) in DCM (10 mL) was added N,N-dimethylammonium iodideand the resulting mixture stirred at room temperature for 16 hrs. Thevolatiles were evaporated in vacuo and the resulting residue waspurified by preparative HPLC, dried in vacuo at 50° C. affording 54 mg(23%) of the title compound isolated as the trifluoroacetate salt.

MS-ESI m/z 354; ¹H NMR (400 MHz, DMSO) δ 0.90 (d, 3H), 0.97 (d, 3H),1.08-1.17 (m, 4H), 1.28-1.53 (m, 4H), 1.72-1.79 (m, 1H), 2.76 (s, 6H),3.14-3.16 (m, 1H), 3.33-3.36 and 3.44-3.47 (2×m, 1H), 4.08-4.15 and4.39-4.42 (2×m, 1H), 4.45 (s, 2H), 7.19 (dd, 1H), 7.54 (d, 1H), 7.69 (s,1H), 7.81 (t, 1H), 9.90 (s, 1H), 11.74 (s, 1H).

Example 101-[3-Acetyl-2-[5-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]octane-6-carbonyl)-1H-indol-3-yl]-2,3-dihydro-imidazol-1-yl]-ethanone

To a solution of imidazole (23 mg, 0.34 mmol) in acetic anhydride at125° C. was added dropwise over 40 min a solution of(1H-Indol-5-yl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone(100 mg, 0.34 mmol) in acetic anhydride (13 mL). The resulting mixturewas heated at 125° C. for 30 min then cooled and solvents evaporated invacuo. The resulting residue was purified by preparative HPLC, dried invacuo at 50° C. to afford 5.4 mg (4%) of the title compound as a solid.

MS-ESI m/z 449; ¹H NMR (400 MHz, DMSO) δ 0.94 (d, 3H), 0.97 (d, 3H),1.08-1.17 (m, 4H), 1.28-1.62 (m, 4H), 1.72-1.79 (m, 1H), 2.05-2.08 (m,6H), 3.14-3.16 (m, 1H), 3.26-3.28 (m, 1H), 3.33-3.36 and 3.63-3.67 (2×m,1H), 4.04-4.06 and 4.61-4.63 (2×m, 1H), 6.33-6.40 (m, 2H), 6.96-7.00 (m,1H), 7.17-7.49 (m, 2H), 7.67-7.82 (m, 1H), 8.94 (s, 1H).

Example 111-Ethyl-3-[5-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]octane-6-carbonyl)-1H-indol-3-yl]-pyrrolidine-2,5-dione

A solution of(1H-Indol-5-yl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone(100 mg, 0.34 mmol) and N-ethylmaleimide (127 mg, 1.01 mmol) in aceticacid (2 mL) was heated at 160° C. employing microwave irradiation for 1hr. The solvents were evaporated in vacuo and the resulting residuepurified by preparative HPLC, dried in vacuo at 50° C. to afford 25 mg(18%) of the title compound as a solid.

MS-ESI m/z 422; ¹H NMR (400 MHz, CDCl₃) δ 0.93-0.96 (m, 3H), 1.01-1.06(m, 3H), 1.13-1.17 (m, 3H), 1.21-1.25 (m, 3H), 1.28-1.44 (m, 3H),1.55-1.64 (m, 1H), 1.73-1.81 (m, 1H), 2.05-2.28 (m, 1H), 2.78-2.87 (m,1H), 3.17-3.34 (m, 1H), 3.57-3.68 (m, 3H), 4.01-4.07 and 4.62-4.64 (2×m,1H), 4.24-4.28 (m, 1H), 7.11-7.12 (m, 1H), 7.22-7.31 (m, 3H), 7.53-7.60(m, 1H), 8.83 (s, 1H).

Example 12(3-Thiazol-2-yl-1H-indol-5-yl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone

To a slurry of(1H-Indol-5-yl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone(300 mg, 1.01 mmol) in benzene (8 mL) under an inert atmosphere ofnitrogen was added methylmagnesium iodide (0.34 mL, 1.01 mmol), afterstirring for 10 mins 2-bromothiazole was added where upon the mixturewas heated at 90° C. for 16 hrs. Water (20 mL) was added and theorganics were extracted with DCM (3×20 mL). The combined organic phaseswere dried (MgSO₄), filtered and evaporated in vacuo. The residue waspurified by preparative HPLC, dried in vacuo at 50° C. affording 48 mg(25%) of the title compound as a solid.

MS-ESI m/z 380; ¹H NMR (300 MHz, CDCl₃) δ 0.93-1.08 (m, 6H), 1.16-1.20(m, 5H), 1.39-1.47 (m, 2H), 1.59-1.64 (m, 1H), 1.80-1.85 (m, 1H),3.21-3.24 (m, 1H), 3.34-3.38 and 3.65-3.69 (2×m, 1H), 4.01-4.03 and4.65-4.68 (2×m, 1H), 7.31-7.35 (m, 2H), 7.48-7.52 (m, 1H), 7.82 (d, 1H),7.91 (d, 1H), 8.34 (s, 1H), 9.77 (s, 1H).

Example 13(3-Iodo-1H-indol-5-yl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone

To a solution of(1H-Indol-5-yl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone(1 g, 3.37 mmol) and potassium hydroxide (364 mg, 6.75 mmol) in DMF (40mL) was added iodine (0.86 g, 3.41 mmol). The reaction mixture wasstirred for 1 hr at room temperature then poured onto water (100 mL),extracted with DCM (3×20 mL). The combined organic phases were washedwith water and brine then dried (MgSO₄), filtered and evaporated invacuo. The resulting solid was dried in vacuo at 50° C. affording 1.18 g(83%) of the title compound.

MS-ESI m/z 423; ¹H NMR (300 MHz, DMSO) δ 0.90 (d, 3H), 0.98 (d, 3H),1.10 (d, 3H), 1.15-1.45 (m, 4H), 1.50-1.54 (m, 1H), 1.75-1.78 (m, 1H),3.15-3.18 (m, 1H), 3.30-3.33 and 3.41-3.45 (2×m, 1H), 3.98-4.00 and4.40-4.42 (2×m, 1H), 7.22-7.42 (m, 2H), 7.44-7.47 (m, 1H), 7.64 (s, 1H),11.73 (s, 1H).

Example 146-(1,3,3-Trimethyl-6-aza-bicyclo[3.2.1]octane-6-carbonyl)-1H-indole-3-carbonitrile

To an ice-cooled slurry of(1H-Indol-6-yl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone(1 g, 3.37 mmol) in acetonitrile (25 mL) was added dropwise a solutionof chlorosulfunylisocyanate (0.48 g, 3.37 mmol). The reaction mixturewas stirred for 1 hr at 0° C. then triethylamine (0.33 g, 3.3 mmol) wasadded dropwise maintaining an internal temperature of 0° C. The reactionmixture was allowed to warm to room temperature over 2 hrs. The solventswere evaporated in vacuo and the residue treated with DCM (10 mL) and anice cold solution of sodium bicarbonate (5%, 10 mL) and the organicswere extracted with DCM (3×20 mL). The combined organic phases weredried (MgSO₄), filtered and evaporated in vacuo. The residue waspurified by preparative HPLC, dried in vacuo at 50° C. affording 182 mg(17%) of the title compound as a solid.

MS-ESI m/z 322; ¹H NMR (400 MHz, DMSO) δ 0.90 (d, 3H), 0.98 (d, 3H),1.09 (s, 3H), 1.15-1.54 (m, 5H), 1.74-1.78 (m, 1H), 3.13-3.16 (m, 1H),3.29-3.32 and 3.44-3.47 (2×m, 1H), 3.94-3.98 and 4.40-4.42 (2×m, 1H),7.27-7.35 (m, 1H), 7.60 (d, 1H), 7.66-7.70 (m, 1H), 8.35-8.37 (m, 1H),12.32 (s, 1H).

The following compound was synthesised employing a similar method to theone described in example 14. MS-ESI No Molecule MW IUPAC Name m/z 14-1

321.42 5-(1,3,3-Trimethyl-6-aza- bicyclo[3.2.1]octane-6-carbonyl)-1H-indole-3- carbonitrile 322

Example 156-(1,3,3-Trimethyl-6-aza-bicyclo[3.2.1]octane-6-carbonyl)-1H-indole-3-carboxylicacid amide

To a solution of6-(1,3,3-Trimethyl-6-aza-bicyclo[3.2.1]octane-6-carbonyl)-1H-indole-3-carbonitrile(65 mg, 0.2 mmol) in 1,4-dioxane (2 mL) was added sodium hydroxidesolution (2 mL, 1M) and hydrogen peroxide (2 mL) and the resultingsolution was heated at 50° C. for 16 hrs. The solvents were evaporatedin vacuo and the residue was purified by preparative HPLC, dried invacuo at 50° C. affording 15 mg (21%) of the title compound as a solid.

MS-ESI m/z 340; ¹H NMR (400 MHz, CDCl₃) δ 0.92 (d, 3H), 0.98 (d, 3H),1.10 (d, 3H), 1.15-1.54 (m, 5H), 1.74-1.79 (m, 1H), 3.18-3.21 (m, 1H),3.25-3.28 and 3.61-3.64 (2×m, 1H), 4.01-4.03 and 4.55-4.58 (2×m, 1H),6.11 (bs, 2H), 7.19-7.23 (m, 1H), 7.34-7.38 (m, 1H), 7.77-7.80 (m, 1H),7.95-7.99 (m, 1H), 10.80 (s, 1H).

Example 16[3-(2H-Tetrazol-5-yl)-1H-indol-6-yl]-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone

A slurry of6-(1,3,3-Trimethyl-6-aza-bicyclo[3.2.1]octane-6-carbonyl)-1H-indole-3-carbonitrile(100 mg, 0.31 mmol), zinc bromide (70 mg, 0.31 mmol) and sodium azide(22 mg, 0.34 mmol) in water (0.65 mL) was heated at 200° C. employingmicrowave irradiation for 6 min. A solution of sodium hydroxide (3 mL,0.25 M) was added and the mixture stirred for 45 min. Filtration of theinorganics followed by acidification of the filtrate with concentratedHCl to pH 1 yielded after filtration crude product which was purified bypreparative HPLC, dried in vacuo at 50° C. affording 6 mg (5%) of thetitle compound as a solid.

MS-ESI m/z 365; ¹H NMR (400 MHz, DMSO) δ 0.92 (d, 3H), 0.99 (d, 3H),1.10 (d, 3H), 1.15-1.55 (m, 5H), 1.74-1.79 (m, 1H), 3.15-3.20 (m, 1H),3.25-3.32 and 3.45-3.48 (2×m, 1H), 4.01-4.03 and 4.41-4.43 (2×m, 1H),7.26-7.35 (m, 1H), 7.61 (d, 1H), 8.15-8.18 (m, 1H), 8.21-8.25 (m, 1H),11.98 (s, 1H).

Example 17N-[3-(1,3,3-Trimethyl-6-aza-bicyclo[3.2.1]octane-6-carbonyl)-1H-indol-7-yl]-acetamide

To a solution of(7-nitro-1H-indol-3-yl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone(730 mg, 2.14 mmol) in MeOH (40 mL) was added palladium on activatedcharcoal (10% Pd, 50% H₂O, 0.2 g). The reaction mixture was stirred for16 hrs under an atmosphere of hydrogen. The catalyst was removed byfiltration and the solvents were evaporated in vacuo and the solid driedin vacuo at 50° C. affording 481 mg (72%) of(7-amino-1H-indol-3-yl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone.To a solution of(7-amino-1H-indol-3-yl)(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone(100 mg, 0.32 mmol) in DCM (1 mL) was added DIPEA (829 mg, 6.4 mmol) andacetic anhydride (327 mg, 3.21 mmol), the solution was stirred at roomtemperature for 1 hr. Solvents were evaporated in vacuo and the residuewas purified by preparative HPLC, dried in vacuo at 50° C. affording 47mg (42%) of the title compound as a solid.

.MS-ESI m/z 354; ¹H NMR (300 MHz, CDCl₃) δ 0.82-1.13 (m, 10H), 1.22-1.54(m, 6H), 1.75-1.78 (m, 1H), 3.10-3.25 (m, 1H), 3.27-3.37 and 3.59-3.66(2×m, 1H), 4.20-4.22 and 4.49-4.52 (2×m, 1H), 6.88-7.01 (m, 1H),7.02-7.08 (m, 1H), 7.40-7.61 (m, 3H), 8.77 (s, 1H), 11.21 (bd, 1H).

Example 18(1-Benzenesulfonyl-1H-indol-5-yl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone

To a solution of(1H-Indol-5-yl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone(1 g, 3.37 mmol) in dry THF (2 mL) at −78° C. under an inert atmosphereof nitrogen was added a solution of n-butyl lithium (2.14 mL, 1.65 M inhexane). Cooling was removed and the solution was allowed to warm toroom temperature with stirring. The solution was cooled to −78° C. whereupon benzenesulphonyl chloride (655 mg, 3.71 mmol) was added and thereaction mixture was stirred for 16 hrs whilst warming to roomtemperature. The reaction was quenched by the addition of sodiumbicarbonate solution (5%, 200 mL) and extracted with DCM (3×50 mL). Thecombined organic phases were washed with water and brine then dried(MgSO₄), filtered and evaporated in vacuo. The resulting solid waspurified by flash column chromatography (mobile phase ethylacetate:heptane, 1:2). Product fractions were combined, evaporated in vacuo,dried in vacuo at 50° C. to afford 1.46 g (99%) of the title compound.

MS-ESI m/z 437; ¹H NMR (300 MHz, CDCl₃) δ 0.94 (d, 3H), 1.02 (d, 3H),1.12-1.17 (m, 3H), 1.24-1.40 (m, 2H), 1.45 (s, 1H), 1.50-1.61 (m, 2H),1.73-1.78 (m, 1H), 3.15-3.25 (m, 1H), 3.26-3.31 and 3.58-3.63 (2×m, 1H),3.96-3.99 and 4.60-4.62 (2×m, 1H), 6.68-6.70 (m, 1H), 7.37-7.47 (m, 3H),7.53-7.63 (m, 3H), 7.84-7.87 (m, 2H), 7.99-8.03 (m, 1H).

Example 19(1-Benzenesulfonyl-2-methyl-1H-indol-5-yl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone

To a solution of(1-Benzenesulfonyl-1H-indol-5-yl)-(1,3,3-trimethyl-6-aza-bicyclo-[3.2.1]oct-6-yl)-methanone(100 mg, 0.23 mmol) in dry THF (2 mL) at −78° C. under an inertatmosphere of nitrogen was added a solution of lithiumN,N-diisopropylamide (0.165 mL, 1.5 M in cyclohexane). The mixture wasstirred for 1 hr at −78° C. then cooling was removed and the solutionwas allowed to warm to room temperature with stirring. The solution wascooled to −78° C. where upon methyl iodide (48 mg, 0.343 mmol) was addedand the reaction mixture was stirred for 16 hrs whilst warming to roomtemperature. The reaction was quenched by the addition of saturatedammonium chloride solution (10 mL) and extracted with DCM (3×10 mL). Thecombined organic phases were dried (MgSO₄), filtered and evaporated invacuo. The residue was purified by preparative HPLC, dried in vacuo at50° C. affording 12 mg (11%) of the title compound as a solid.

MS-ESI m/z 451; ¹H NMR (300 MHz, CDCl₃) δ 0.94 (d, 3H), 1.04 (d, 3H),1.13-1.15 (m, 3H), 1.25-1.40 (m, 2H), 1.45 (s, 1H), 1.55-1.61 (m, 2H),1.74-1.80 (m, 1H), 2.60 (s, 3H), 3.17-3.25 (m, 1H), 3.27-3.31 and3.59-3.64 (2×m, 1H), 4.00-4.02 and 4.61-4.63 (2×m, 1H), 6.38 (s, 1H),7.32-7.58 (m, 5H), 7.74-7.77 (m, 2H), 8.16-8.20 (m, 1H).

Example 20(1-methyl-1H-indol-5-yl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone

To a solution of(1H-Indol-5-yl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone(500 mg, 1.69 mmol) in dry DMF (10 mL) at room temperature under aninert atmosphere of nitrogen was added sodium hydride (53 mg, 2.19 mmol,60% dispersion in oil), after stirring for 30 min methyl iodide (263 mg,1.85 mmol) was added and the reaction mixture was stirred for 16 hrs at60° C. The reaction was quenched by the addition of water (20 mL)followed by extraction with DCM (3×50 mL). The combined organic phaseswere dried (MgSO₄), filtered and evaporated in vacuo. The resultingsolid was purified by preparative HPLC, dried in vacuo at 50° C.affording 261 mg (50%) of the title compound as a solid.

MS-ESI m/z 311; ¹H NMR (300 MHz, DMSO) δ 0.89 (d, 3H), 0.96 (d, 3H),1.07-1.21 (m, 4H), 1.23-1.53 (m, 4H), 1.72-1.78 (m, 1H), 3.10-3.15 (m,1H), 3.34-3.47 (m, 1H), 3.80 (d, 3H), 4.01-4.04 and 4.38-4.40 (2×m, 1H),6.48-6.50 (m, 1H), 7.18-7.28 (m, 1H), 7.39 (d, 1H), 7.43-7.48 (m, 1H),7.64 (d, 1H).

The following compounds were synthesised employing a similar method tothe ones described in example 20. MS- ESI No Molecule MW IUPAC Name m/z20-1 

386.54 (1-Benzyl-1H-indol-5-yl)- (1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)- methanone 387 20-2 

382.50 [6-(1,3,3-Trimethyl-6-aza- bicyclo[3.2.1]octane-6-carbonyl)-indol-1-yl]-acetic acid ethyl ester 383 20-3 

368.52 [1-(2-Ethoxy-ethyl)-1H-indol- 6-yl]-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)- methanone 369 20-4 

398.54 {1-[2-(2-Methoxy-ethoxy)- ethyl]-1H-indol-6-yl}-(1,3,3-trimethyl-6-aza- bicyclo[3.2.1]oct-6-yl)- methanone 399 20-5 

396.53 3-[5-(1,3,3-Trimethyl-6-aza- bicyclo[3.2.1]octane-6-carbonyl)-indol-1-yl]- propionic acid ethyl ester 397 20-6 

400.56 (1-Phenethyl-1H-indol-5-yl)- (1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)- methanone 401 20-7 

380.53 [1-(Tetrahydro-furan-2- ylmethyl)-1H-indol-5-yl]-(1,3,3-trimethyl-6-aza- bicyclo[3.2.1]oct-6-yl)- methanone 381 20-8 

353.46 2-[5-(1,3,3-Trimethyl-6-aza- bicyclo[3.2.1]octane-6-carbonyl)-indol-1-yl]- acetamide 354 20-9 

470.53 [1-(4-Trifluoromethoxy- benzyl)-1H-indol-5-yl]-(1,3,3-trimethyl-6-aza- bicyclo[3.2.1]oct-6-yl)- methanone 471 20-10

444.57 3-[5-(1,3,3-Trimethyl-6-aza- bicyclo[3.2.1]octane-6-carbonyl)-indol-1-ylmethyl]- benzoic acid methyl ester 445 20-11

411.55 4-[5-(1,3,3-Trimethyl-6-aza- bicyclo[3.2.1]octane-6-carbonyl)-indol-1-ylmethyl]- benzonitrile 412

EXAMPLES Compounds of General Formula (VIII)

The following examples and general procedures refer to intermediatecompounds and final products for general formula (VIII) identified inthe specification and in the synthesis schemes. The preparation of thecompounds of general formula (VIII) of the present invention isdescribed in detail using the following examples. Occasionally, thereaction may not be applicable as described to each compound includedwithin the disclosed scope of the invention. The compounds for whichthis occurs will be readily recognised by those skilled in the art. Inthese cases the reactions can be successfully performed by conventionalmodifications known to those skilled in the art, that is, by appropriateprotection of interfering groups, by changing to other conventionalreagents, or by routine modification of reaction conditions.Alternatively, other reactions disclosed herein or otherwiseconventional will be applicable to the preparation of the correspondingcompounds of the invention. In all preparative methods, all startingmaterials are known or may easily be prepared from known startingmaterials. The structures of the compounds are confirmed by eitherelemental analysis or nuclear magnetic resonance (NMR), where peaksassigned to characteristic protons in the title compounds are presentedwhere appropriate. ¹H NMR shifts (6H) are given in parts per million(ppm) down field from tetramethylsilane as internal reference standard.M.p.: is melting point and is given in ° C. and is not corrected. Columnchromatography was carried out using the technique described by W. C.Still et al., J. Org. Chem. 43: 2923 (1978) on Merck silica gel 60 (Art.9385). HPLC analyses are performed using 5 μm C18 4×250 mm column elutedwith various mixtures of water and acetonitrile, flow=1 ml/min, asdescribed in the experimental section.

The abbreviations as used in the examples have the following meaning:

TLC: thin layer chromatography

CDCl₃: deuterio chloroform

CD₃OD: tetradeuterio methanol

DMSO-d₆: hexadeuterio dimethylsulfoxide

DMSO: dimethylsulfoxide

THF: tetrahydrofuran

DMF: N,N-dimethylformamide

HOBT: 1-hydroxy-benzotriazole

EDAC: 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide, hydrochloride

min: minutes

hrs: hours

The compounds of the invention are prepared as illustrated in thefollowing reaction scheme 1:

General Method:

By allowing a 2-halo-3-oxo-propionic acid ester (I) wherein Y is halo,R¹ is C₁-C₆alkyl, aryl, arylC₁-C₆alkyl and R² is as defined above toreact with an amide (II), wherein R³ is as defined above and X is O orS, in a solvent such as ethanol and the like affording an thiazole,oxazol or imidazol carboxylic acid ester (III), wherein R² and R³ is asdefined above. The thiazole, oxazol or imidazol carboxylic acid ester(III) is hydrolysed with base affording thiazole, oxazol or imidazolcarboxylic acid (V), wherein R² and R³ are as defined above. Thethiazole, oxazol or imidazol carboxylic acid (V) can also be obtainedfrom the corresponding bromo or iodo substituted thiazole, oxazol orimidazol (IV) via halogen lithium exchange followed by reaction withcarbon dioxide in a solvent such as THF. The thiazole, oxazol orimidazol carboxylic acid (V) is coupled with an amine (VI), wherein R⁵and R⁶ are as defined above, under standard amide forming conditions(e.g. HOBT, EDAC and DIPEA in dry THF) affording thiazole, oxazol orimidazol (VII), wherein R², R³, R⁵ and R⁶ are as defined above.

Example 14-Methyl-2-phenyl-thiazol-5-yl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone

A solution of 4-methyl-2-phenyl-1,3-thiazole-5-carboxylic acid (0.44 g,2.00 mmol), HOBT (0.297 g, 2.2 mmol), EDAC (0.42 g, 2.2 mmol) anddi-isopropyl ethyl amine (DIPEA) (383 μl, 2.2 mmol) in dry THF (30 ml)was stirred for 30 minutes and 1,3,3-trimethyl-6-azabicyclo[3.2.1]octane(0.34 g, 2.2 mmol) was added. The mixture was stirred for 16 hrs. atroom temperature. The mixture was added water (30 ml) and extracted withETOAc (2×50 ml), dried (MgSO₄), filtered and evaporated in vacuoaffording 0.67 g (94%) of the title compounds as an oil.

¹H-NMR (400 MHz, CDCl₃) δ 0.94-1.14 (m, 9H), 1.26-1.8 (m, 5H), 2.25 (m,1H), 2.55 (d, 3H), 3.26 (m, 1H), 3.44 and 3.66 (2×d, 1H), 4.18 and 4.60(2×t, 1H), 7.44 (m, 3H), 7.92 (m, 2H).

Example 2(2,4-Dimethyl-thiazol-5-yl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone

A solution of 2,4-dimethyl-1,3-thiazole-5-carboxylic acid (0.47 g, 3.00mmol), HOBT (0.46 g, 3.3 mmol), EDAC (0.63 g, 3.3 mmol) and di-isopropylethyl amine (DIPEA) (575 μl, 3.3 mmol) in dry THF (50 ml) was stirredfor 40 minutes and 1,3,3-trimethyl-6-azabicyclo-[3.2.1]octane (0.51 g,3.3 mmol) was added. The mixture was stirred for 16 hrs. at roomtemperature. The mixture was added water (30 ml) and extracted withETOAc (2×50 ml), dried (MgSO₄), filtered and evaporated in vacuoaffording 0.145 g (17%) of the title compounds as an oil.

¹H-NMR (400 MHz, CDCl₃) δ 0.97-1.15 (m, 9.5H), 1.35-1.63 (m, 4.5H), 2.17(dd, 1H), 2.53 (d, 3H), 2.89 (d, 3H), 3.24 (m, 1H), 3.4 and 3.67 (2×d,1H), 4.10 and 4.58 (2×t, 1H).

Example 3(4-Methyl-2-pyrazin-2-yl-thiazol-5-yl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone

A solution of 4-methyl-2-(2-pyrazinyl)-1,3-thiazole-5-5-carboxylic acid(0.22 g, 1.00 mmol), HOBT (0.17 g, 1.1 mmol), EDAC (0.21 g, 1.1 mmol)and di-isopropyl ethyl amine (DIPEA) (192 μl, 1.1 mmol) in dry THF (10ml) was stirred for 30 minutes and1,3,3-trimethyl-6-azabicyclo[3.2.1]octane (0.17 g, 1.1 mmol) was added.The mixture was stirred for 16 hrs. at room temperature. The mixture wasadded water (30 ml) and extracted with ETOAc (2×50 ml), dried (MgSO₄),filtered and evaporated in vacuo. affording 0.345 g (97%) of the titlecompounds as an oil.

The following compounds were prepared in a similar way as described inExample 3 above.

Example 4[4-Methyl-2-(4-trifluoromethyl-phenyl)-thiazol-5-yl]-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone

¹H-NMR (400 MHz, CDCl₃) δ 0.94 (m, 3H), 1.07 (t, 3H), 1.17 (t, 3H),1.32-1.84 (m, 4.5H), 2.25 (m, 0.5H), 2.58 (d, 3H), 2.86 (d, 0.5H), 3.23(q, 1H), 3.4 (d, 0.5H), 3.66 (d, 0.5H), 3.80 (m, 0.5H), 4.18 (m, 0.5H),4.60 (m, 0.5H), 7.68 (t, 2H), 8.04 (d, 2H).

Example 5(1H-Imidazol-4-yl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone

¹H-NMR (400 MHz, CDCl₃) δ 0.94-0.99 (m, 6H), 1.15 (d, 3H), 1.37 (d, 1H),1.44-1.52 (m, 2H), 1.60 (d, 1H), 1.74 (m, 0.5H), 1.83 (m, 0.5H), 2.09(t, 1H), 3.29 (d, 0.5H), 3.45 (d, 0.5H), 3.61 (d, 0.5H), 3.77 (d, 0.5H),4.68 (m, 0.5H), 4.80 (bs, 0.5H), 7.49 (d, 1H), 7.69 (d, 1H), 11.45 (bs,1H).

Example 6(3-Aza-bicyclo[3.2.2]non-3-yl)-(4-methyl-2-phenyl-thiazol-5-yl)-methanone

¹H-NMR (400 MHz, CDCl₃) δ 1.70 (bs, 10H), 2.48 (s, 3H), 3.75 (bs, 4H),7.43 (t, 3H), 7.91 (m, 2H).

Example 7(1-Methyl-1H-imidazol-4-yl)-(1,33-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone

¹H-NMR (400 MHz, CDCl₃) δ 0.93 (s, 3H), 0.98 (d, 3H), 1.11 (s, 3H),1.28-1.46 (m, 3H), 1.55 (d, 1H), 1.69 (m, 0.5H), 1.80 (m, 0.5H),2.05-2.16 (m, 1H), 3.22 (dd, 0.5H), 3.62 (dq, 1H), 3.71 (s, 3H), 4.12(d, 0.5H), 4.64 (m, 0.5H), 5.36 (m, 0.5H), 7.39 (d, 1H), 7.58 (d, 1H).

Example 8[1-(6-Methyl-pyridin-2-yl)-1H-imidazol-4-yl]-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone

¹H-NMR (400 MHz, CDCl₃) δ 0.94 (s, 3H), 1.00 (d, 3H), 1.13 (d, 3H),1.25-1.44 (m, 3H), 1.56 (m, 1H), 1.72 (m, 0.5H), 1.83 (m, 0.5H),2.08-2.18 (m, 1H), 2.57 (s, 3H), 3.26 (d, 0.5H), 3.65 (q, 1H), 4.16 (d,0.5H), 4.68 (m, 0.5H), 5.42 (m, 0.5H), 7.12 (d, 1H), 7.18 (d, 1H), 7.72(t, 1H), 8.24 (s, 1H), 8.35 (s, 1H).

Example 9[1-(4-Chloro-benzyl)-5-methyl-1H-imidazol-4-yl]-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone

¹H-NMR (300 MHz, CDCl₃) δ 0.93 (s, 3H), 1.01 (d, 3H), 1.10 (d, 3H),1.26-1.46 (m, 3H), 1.55 (d, 1H), 1.69 (m, 0.5H), 1.79 (m, 0.5H),2.04-2.18 (m, 1H), 2.41 (d, 3H), 3.22 (d, 0.5H), 3.59 (d, 1H), 4.06 (d,0.5H), 4.64 (m, 0.5H), 5.05 (s, 2H), 5.15 (m, 0.5H), 7.00 (d, 2H), 7.32(d, 2H), 7.43 (d, 1H).

Pharmacological Methods

11βHSD1 Enzyme Assay

Materials

³H-cortisone and anti-rabbit Ig coated scintillation proximity assay(SPA) beads were purchased from Amersham Pharmacia Biotech, β-NADPH wasfrom Sigma and rabbit anti-cortisol antibodies were from Fitzgerald. Anextract of yeast transformed with h-11βHSD1 (Hult et al., FEBS Lett.,441, 25 (1998)) was used as the source of enzyme. The test compoundswere dissolved in DMSO (10 mM). All dilutions were performed in a buffercontaining 50 mM TRIS-HCl (Sigma Chemical Co), 4 mM EDTA (Sigma ChemicalCo), 0.1% BSA (Sigma Chemical Co), 0.01% Tween-20 (Sigma Chemical Co)and 0.005% bacitracin (Novo Nordisk A/S), pH=7.4. Optiplate 96 wellsplates were supplied by Packard. The amount of ³H-cortisol bound to theSPA beads was measured on TopCount NXT, Packard.

Methods

h-11βHSD1, 120 nM ³H-cortisone, 4 mM β-NADPH, antibody (1:200), serialdilutions of test compound and SPA particles (2 mg/well) were added tothe wells. The reaction was initiated by mixing the different componentsand was allowed to proceed under shaking for 60 min at 30° C. Thereaction was stopped be the addition of 10 fold excess of a stoppingbuffer containing 500 μM carbenoxolone and 1 μM cortisone. Data wasanalysed using GraphPad Prism software. TABLE 1 Inhibition of 11βHSD1 bycompounds of the invention 11βHSD1 Formula Example No. IC₅₀ values (I) 10.56 μM (I) 2 120 μM (III) 1 0.04 μM (V) 1 45 nM (VI) 1 6 nM (VII) 2 118nM

1. A method of modulating of the activity of 11βHSD1, or inhibiting11βHSD1, comprising administering to a patient in need of such method atherapeutically effective amount of a substituted amide, a prodrugthereof, or a salt thereof with a pharmaceutically acceptable acid orbase, or optical isomer or mixture of optical isomers, racemic mixtureor tautomeric forms thereof.
 2. A method for the treatment, preventionand/or prophylaxis of any disorder and disease where it is desirable tomodulate the activity of 11βHSD1, or inhibit 11βHSD1, comprisingadministering to a patient in need of such method a therapeuticallyeffective amount of a substituted amide, a prodrug thereof, or a saltthereof with a pharmaceutically acceptable acid or base, or opticalisomer or mixture of optical isomers, racemic mixture or any tautomericforms thereof.
 3. The method according to claim 2, wherein thesubstituted amide or a prodrug thereof is of formula (I)

wherein R¹ is C₃-C₁₀cycloalkyl, C₃-C₁₀hetcycloalkyl, C₁-C₈alkyl, aryl,hetaryl, arylC₁-C₆alkyl or hetarylC₁-C₆alkyl, wherein the cycloalkyl,hetcycloalkyl, alkyl, arylalkyl and hetarylalkyl groups independentlyare optionally substituted with one or more of R⁴. R² is hydrogen,C₁-C₈alkyl, aryl, hetaryl, arylC₁-C₆alkyl, C₃-C₁₀cycloalkylC₁-C₆alkyl,C₁-C₆alkylcarboxyC₁-C₆alkyl wherein the alkyl, aryl and cycloalkylgroups independently are optionally substituted with one or more of R⁵;or R¹ and R² together with the nitrogen to which they are attached, areforming a saturated or partially saturated cyclic, bicyclic or tricyclicring system containing from 4 to 10 carbon atoms and from 0 to 2additional heteroatoms selected from nitrogen, oxygen or sulphur, thering system optionally being substituted with at least one ofC₁-C₈alkyl, aryl, hetaryl, arylC₁-C₆alkyl, hetarylC₁-C₆alkyl, hydroxy,oxo, cyano, C₁-C₆alkyloxy, arylC₁-C₆alkyloxy, hetarylC₁-C₆alkyloxy,C₁-C₆alkyloxyC₁-C₆alkyl, C₁-C₆alkylcarbonyl, arylcarbonyl,hetarylcarbonyl, arylC₁-C₆alkylcarbonyl, hetarylC₁-C₆alkylcarbonyl,C₁-C₆alkylcarboxy, arylcarboxy or arylC₁-C₆alkylcarboxy wherein thealkyl and aryl groups independently are optionally substituted with oneor more of R¹⁴; R³ is C₁-C₈alkyl, C₁-C₆alkenyl, C₁-C₆alkynyl,C₃-C₁₀cycloalkyl, C₃-C₁₀hetcycloalkyl, aryl, hetaryl, arylC₁-C₆alkyl,C₁-C₆alkyloxyC₁-C₆alkyl, hetarylC₁-C₆alkyl, aryl-R⁶—C₁-C₆alkyl,hetaryl-R⁶—C₁-C₆alkyl or arylC₁-C₆alkyl-R⁶—C₁-C₆alkyl wherein the alkyl,cycloalkyl, hetcycloalkyl, alkenyl, alkynyl, aryl and hetaryl groupsindependently are optionally substituted with one or more of R⁷; R⁴ andR⁵ independently are hydrogen, hydroxy, oxo, cyano, halo, methylendioxo,NR⁸R⁹, C₁-C₈alkyl, C₁-C₆alkyloxy, trihalomethyl, trihalomethyloxy,C₃-C₁₀cycloalkyl, C₃-C₁₀hetcycloalkyl, C₃-C₁₀cycloalkenyl, aryl,hetaryl, hetarylSO_(n), arylC₁-C₆alkyloxy, hetarylC₁-C₆alkyloxy,C₁-C₆alkyl-R⁶—C₁-C₆alkyl, arylC₁-C₆alkyl-R⁶—C₁-C₆alkyl,C₁-C₆alkylcarbonyl, arylcarbonyl, arylC₁-C₆alkylcarbonyl,hetarylcarbonyl, hetarylC₁-C₆alkyl-carbonyl, C₁-C₆alkylSO_(n),C₁-C₆alkyl-carboxy, arylcarboxy, hetarylcarboxy, arylC₁-C₆alkylcarboxyor hetarylC₁-C₆alkylcarboxy wherein the alkyl, cycloalkyl,hetcycloalkyl, aryl and hetaryl groups independently are optionallysubstituted with one or more of R¹⁵; R⁶ is oxygen, sulphur, SO_(n) orNR¹⁶; R⁷ is hydrogen, halo, hydroxy, cyano, nitro, COOR¹⁷, C₁-C₈alkyl,C₃-C₁₀cycloalkyl, C₃-C₁₀hetcycloalkyl, methylendioxo, trihalomethyl,trihalomethyloxy, aryl, arylC₁-C₆alkyl, C₁-C₆alkyloxy,C₁-C₆alkyloxyC₁-C₆alkyl, aryloxy, arylC₁-C₆alkyloxy, aryloxyC₁-C₆alkyl,arylC₁-C₆alkyloxyC₁-C₆alkyl, hetaryl, hetarylC₁-C₆alkyl, hetaryloxy,hetarylC₁-C₆alkyloxy, hetaryloxyC₁-C₆alkyl,hetarylC₁-C₆alkyl-oxyC₁-C₆alkyl, NR⁸R⁹, SO₂NR⁸R⁹,NR⁴R⁵carbonylC₁-C₆alkyl, arylthio, hetarylthio, R¹⁸carbonylNR⁸,arylSO_(n), hetarylSO_(n), R¹⁹SO_(m)NR⁸, arylthioC₁-C₆alkyl,hetarylthioC₁-C₆alkyl or arylC₁-C₆alkylR⁶C₁-C₆alkyl; wherein the aryland hetaryl groups independently are optionally substituted with one ormore R¹⁰; R⁸ and R⁹ independently are hydrogen, C₁-C₈alkyl, aryl,hetaryl, arylC₁-C₆alkyl or hetarylC₁-C₆alkyl wherein the alkyl, aryl andhetaryl groups independently are optionally substituted with one or moreof R¹¹; or R⁸ and R⁹ together with the nitrogen to which they areattached, are forming a saturated or partially saturated cyclic,bicyclic or tricyclic ring system containing from 4 to 10 carbon atomsand from 0 to 2 additional heteroatoms selected from nitrogen, oxygen orsulfur, the ring system optionally being substituted with at least onehalo, cyano, C₁-C₈alkyl, aryl, hetaryl, arylC₁-C₆alkyl,hetarylC₁-C₆alkyl, hydroxy, oxo, C₁-C₆alkyloxy, arylC₁-C₆alkyloxy,hetarylC₁-C₆alkyloxy, C₁-C₆alkyloxyC₁-C₆alkyl, C₁-C₆alkyl-carbonyl,arylcarbonyl, hetarylcarbonyl, arylC₁-C₆alkylcarbonyl,hetarylC₁-C₆alkylcarbonyl, C₁-C₆alkylcarboxy, arylcarboxy,hetarylcarboxy, arylC₁-C₆alkylcarboxy or hetarylC₁-C₆alkylcarboxy; R¹⁰and R¹¹ independently are hydrogen, hydroxy, oxo, halo, cyano, nitro,C₁-C₈alkyl, C₁-C₆alkyloxy, NR¹²R¹³, methylendioxo, trihalomethyl ortrihalomethyloxy; R¹² and R¹³ independently are hydrogen, C₁-C₈alkyl orarylC₁-C₆alkyl; R¹⁴ is hydrogen, halo, hydroxy, oxo, nitro, cyano,C₁-C₈alkyl, C₁-C₆alkyloxy or aryloxy; R¹⁵ is hydrogen, halo, hydroxy,oxo, nitro, cyano, CONR⁸R⁹ or COOR¹⁷; R¹⁶ is hydrogen, C₁-C₈alkyl,C₃-C₁₀cycloalkyl, C₃-C₁₀hetcycloalkyl, aryl, arylC₁-C₆alkyl, hetaryl,hetarylC₁-C₆alkyl, alkylcarbonyl, arylcarbonyl, arylC₁-C₆alkylcarbonyl,aryloxyC₁-C₆alkyl, hetaryloxyC₁-C₆alkyl, arylthioC₁-C₆alkyl orhetarylthioC₁-C₆alkyl; wherein the alkyl, cycloalkyl, hetcycloalkyl,aryl and hetaryl groups independently are optionally substituted withone or more of R¹⁰; R¹⁷ is hydrogen, C₁-C₈alkyl, aryl or arylC₁-C₆alkyl;R¹⁸ is C₁-C₆alkyl, C₂-C₆alkenyl, aryl, arylC₁-C₆alkyl, hetaryl,hetarylC₁-C₆alkyl, C₃-C₁₀cycloalkyl, C₃-C₁₀hetcycloalkyl, C₁-C₆alkyloxy,aryloxy, arylC₁-C₆alkyloxy, arylC₁-C₆alkyloxyC₁-C₆alkyl, hetaryloxy,hetarylC₁-C₆alkyloxy, hetarylC₁-C₆alkyloxyC₁-C₆alkyl or R⁸R⁹NC₁-C₆alkylwherein the alkyl, alkenyl, cycloalkyl, hetcycloalkyl, aryl and hetarylgroups are optionally substituted with R¹⁵; R¹⁹ is C₁-C₆alkyl,C₃-C₁₀cycloalkyl, C₃-C₁₀hetcycloalkyl, aryl, arylC₁-C₆alkyl, hetaryl,hetarylC₁-C₆alkyl; m is 1 or 2; n is 0, 1 or 2; or a salt thereof with apharmaceutically acceptable acid or base, or optical isomer or mixtureof optical isomers, racemic mixture, or tautomeric forms thereof.
 4. Themethod according to claim 3, wherein the substituted amide or a prodrugthereof is of formula (I)

wherein R¹ is C₃-C₁₀cycloalkyl, C₃-C₁₀hetcycloalkyl, C₁-C₈alkyl, aryl,hetaryl, arylC₁-C₆alkyl or hetarylC₁-C₆alkyl, wherein the cycloalkyl,hetcycloalkyl, alkyl, arylalkyl and hetarylalkyl groups independentlyare optionally substituted with one or more of R⁴; R² is hydrogen,C₁-C₈alkyl, aryl, hetaryl, arylC₁-C₆alkyl, C₃-C₁₀cycloalkylC₁-C₆alkyl,C₁-C₆alkylcarboxyC₁-C₆alkyl wherein the alkyl, aryl and cycloalkylgroups independently are optionally substituted with one or more of R⁵;or R¹ and R² are together with the nitrogen to which they are attached,are forming a saturated or partially saturated cyclic, bicyclic ortricyclic ring system containing from 4 to 10 carbon atoms and from 0 to2 additional heteroatoms selected from nitrogen, oxygen or sulphur, thering system optionally being substituted with at least one ofC₁-C₈alkyl, aryl, hetaryl, arylC₁-C₆alkyl, hetarylC₁-C₆alkyl, hydroxy,oxo, cyano, C₁-C₆alkyloxy, arylC₁-C₆alkyloxy, hetarylC₁-C₆alkyloxy,C₁-C₆alkyloxyC₁-C₆alkyl, C₁-C₆alkylcarbonyl, arylcarbonyl,hetarylcarbonyl, arylC₁-C₆alkylcarbonyl, hetarylC₁-C₆alkylcarbonyl,C₁-C₆alkylcarboxy, arylcarboxy or arylC₁₋₆alkylcarboxy wherein the alkyland aryl groups independently are optionally substituted with one ormore of R¹⁴; R³ is C₁-C₈alkyl, C₁-C₆alkenyl, C₁-C₆alkynyl,C₃-C₁₀cycloalkyl, C₃-C₁₀hetcycloalkyl, aryl, hetaryl, arylC₁-C₆alkyl,C₁-C₆alkyloxyC₁-C₆alkyl, hetarylC₁-C₆alkyl, aryl-R⁶—C₁-C₆alkyl,hetaryl-R⁶—C₁-C₆alkyl or arylC₁-C₆alkyl-R⁶—C₁-C₆alkyl wherein the alkyl,cycloalkyl, hetcycloalkyl, alkenyl, alkynyl, aryl and hetaryl groupsindependently are optionally substituted with one or more of R⁷; R⁴ andR⁵ independently are hydrogen, hydroxy, oxo, cyano, halo, methylendioxo,NR⁸R⁹, C₁-C₈alkyl, C₁-C₆alkyloxy, trihalomethyl, trihalomethyloxy,C₃-C₁₀cycloalkyl, C₃-C₁₀hetcycloalkyl, C₃-C₁₀cycloalkenyl, aryl,hetaryl, hetarylSO_(n), arylC₁-C₆alkyloxy, hetarylC₁-C₆alkyloxy,C₁-C₆alkyl-R⁶—C₁-C₆alkyl, arylC₁-C₆alkyl-R⁶—C₁-C₆alkyl,C₁-C₆alkylcarbonyl, arylcarbonyl, arylC₁-C₆alkylcarbonyl,hetarylcarbonyl, hetarylC₁-C₆alkyl-carbonyl, C₁-C₆alkylSO_(n),C₁-C₆alkyl-carboxy, arylcarboxy, hetarylcarboxy, arylC₁-C₆alkylcarboxyor hetarylC₁-C₆alkylcarboxy wherein the alkyl, cycloalkyl,hetcycloalkyl, aryl and hetaryl groups independently are optionallysubstituted with one or more of R¹⁵; R⁶ is oxygen, sulphur, SO_(n),NR¹⁶; R⁷ is hydrogen, halo, hydroxyl, cyano, nitro, COOR⁷, C₁-C₈alkyl,C₃-C₁₀cycloalkyl, C₃-C₁₀hetcycloalkyl, methylendioxo, trihalomethyl,trihalomethyloxy, aryl, arylC₁-C₆alkyl, C₁-C₆alkyloxy,C₁-C₆alkyloxyC₁-C₆alkyl, aryloxy, aryloxyC₁-C₆alkyl,arylC₁-C₆alkyloxyC₁-C₆alkyl, hetaryl, hetarylC₁-C₆alkyl, hetaryloxy,hetarylC₁-C₆alkyloxy, hetaryloxyC₁-C₆alkyl,hetarylC₁-C₆alkyloxyC₁-C₆alkyl, NR⁸R⁹, SO₂NR⁸R⁹, NR⁴R⁵carbonylalkyl,arylcarbonylNR⁸, arylthio, hetarylthio, arylSO_(n), hetarylSO_(n),arylSO_(m)NR⁸, arylthioC₁-C₆alkyl, hetarylthioC₁-C₆alkyl orarylC₁-C₆alkylR⁶C₁-C₆alkyl; wherein the aryl and hetaryl groupsindependently are optionally substituted with one or more R¹⁰; R⁸ and R⁹independently are hydrogen, C₁-C₈alkyl, aryl, hetaryl, arylC₁-C₆alkyl orhetarylC₁-C₆alkyl wherein the alkyl, aryl and hetaryl groupsindependently are optionally substituted with one or more of R¹¹; or R⁸and R⁹ together with the nitrogen to which they are attached, areforming a saturated or partially saturated cyclic, bicyclic or tricyclicring system containing from 4 to 10 carbon atoms and from 0 to 2additional heteroatoms selected from nitrogen, oxygen or sulfur, thering system optionally being substituted with at least one C₁-C₈alkyl,aryl, hetaryl, arylC₁-C₆alkyl, hetarylC₁-C₆alkyl, hydroxy, oxo,C₁-C₆alkyloxy, arylC₁-C₆alkyloxy, hetarylC₁-C₆alkyloxy,C₁-C₆alkyloxyC₁-C₆alkyl, C₁-C₆alkylcarbonyl, arylcarbonyl,hetarylcarbonyl, arylC₁-C₆alkylcarbonyl, hetarylC₁-C₆alkylcarbonyl,C₁-C₆alkylcarboxy, arylcarboxy, hetarylcarboxy, arylC₁-C₆alkyl-carboxyor hetarylC₁-C₆alkylcarboxy; R¹⁰ and R¹¹ independently are hydrogen,hydroxy, oxo, halo, cyano, nitro, C₁-C₈alkyl, C₁-C₆alkyloxy, NR¹²R¹³,methylendioxo, trihalomethyl or trihalomethyloxy; R¹² and R¹³independently are hydrogen, C₁-C₈alkyl or arylC₁-C₆alkyl; R¹⁴ ishydrogen, halo, hydroxy, oxo, nitro, cyano, C₁-C₈alkyl, C₁-C₆alkyloxy oraryloxy; R¹⁵ is hydrogen, halo, hydroxy, oxo, nitro, cyano or COOR¹⁷;R¹⁶ is hydrogen, C₁-C₈alkyl, C₃-C₁₀cycloalkyl, C₃-C₁₀hetcycloalkyl,aryl, arylC₁-C₆alkyl, hetaryl, hetarylC₁-C₆alkyl, alkylcarbonyl,arylcarbonyl, arylC₁-C₆alkylcarbonyl, aryloxyC₁-C₆alkyl,hetaryloxyC₁-C₆alkyl, arylthioC₁-C₆alkyl or hetarylthioC₁-C₆alkyl;wherein the alkyl, cycloalkyl, hetcycloalkyl, aryl and hetaryl groupsindependently are optionally substituted with one or more of R¹⁰; R¹⁷ ishydrogen, C₁-C₈alkyl, aryl or arylC₁-C₆alkyl; m is 1 or 2; n is 0, 1 or2; or a salt thereof with a pharmaceutically acceptable acid or base, oroptical isomer or mixture of optical isomers, racemic mixture, ortautomeric forms thereof.
 5. The method according to claim 3, wherein R¹is C₃-C₁₀cycloalkyl, C₃-C₁₀hetcycloalkyl, wherein the cycloalkyl andhetcycloalkyl groups independently are optionally substituted with oneor more of R⁴.
 6. The method according to claim 3, wherein R² ishydrogen or C₁-C₈alkyl, wherein the alkyl group is optionallysubstituted with one or more of R⁵.
 7. The method according to claim 3,wherein R¹ and R² together with the nitrogen to which they are attached,are forming a saturated or partially saturated cyclic, bicyclic ortricyclic ring system containing from 4 to 10 carbon atoms and from 0 to2 additional heteroatoms selected from nitrogen, oxygen or sulphur, thering system optionally being substituted with at least one ofC₁-C₈alkyl, aryl, hetaryl, arylC₁-C₆alkyl, hetarylC₁-C₆alkyl, hydroxy,oxo, cyano, C₁-C₆alkyloxy, arylC₁-C₆alkyloxy, hetarylC₁-C₆alkyloxy,C₁-C₆alkyloxyC₁-C₆alkyl, C₁-C₆alkylcarbonyl, arylcarbonyl,hetarylcarbonyl, arylC₁-C₆alkylcarbonyl, hetarylC₁-C₆alkylcarbonyl,C₁-C₆alkylcarboxy, arylcarboxy or arylC₁-C₆alkylcarboxy wherein thealkyl and aryl groups independently are optionally substituted with oneor more of R¹⁴.
 8. The method according to claim 3, wherein R³ isC₃-C₁₀cycloalkyl, C₃-C₁₀hetcycloalkyl, aryl, hetaryl, arylC₁-C₆alkyl,hetarylC₁-C₆alkyl, aryl-R⁶—C₁-C₆alkyl, hetaryl-R⁶—C₁-C₆alkyl orarylC₁-C₆alkyl-R⁶—C₁-C₆alkyl wherein the alkyl, cycloalkyl,hetcycloalkyl, aryl and hetaryl groups independently are optionallysubstituted with one or more of R⁷.
 9. The method according to claim 3,wherein R⁴ and R⁵ independently are hydrogen, hydroxy, oxo, halo,C₁-C₈alkyl, wherein the alkyl group is optionally substituted with oneor more of R¹⁵.
 10. The method according to claim 3, wherein R⁵ isoxygen.
 11. The method according to claim 3, wherein R⁷ is hydrogen,halo, hydroxy, cyano, C₁-C₈alkyl, C₃-C₁₀cycloalkyl, C₃-C₁₀hetcycloalkyl,trihalomethyl, aryl, arylC₁-C₆alkyl, C₁-C₆alkyloxy,C₁-C₆alkyloxyC₁-C₆alkyl, aryloxy, arylC₁-C₆alkyloxy, aryloxyC₁-C₆alkyl,arylC₁-C₆alkyloxyC₁-C₆alkyl, hetaryl, hetarylC₁-C₆alkyl, hetaryloxy,hetarylC₁-C₆alkyloxy, hetaryloxyC₁-C₆alkyl,hetarylC₁-C₆alkyl-oxyC₁-C₆alkyl, NR⁸R⁹, NR⁴R⁵carbonylC₁-C₆alkyl,R¹⁸carbonylNR⁸, R¹⁹SO_(m)NR⁸, wherein the aryl and hetaryl groupsindependently are optionally substituted with one or more R¹⁰.
 12. Themethod according to claim 3, wherein R⁸ and R⁹ together with thenitrogen to which they are attached, are forming a saturated orpartially saturated cyclic, bicyclic or tricyclic ring system containingfrom 4 to 10 carbon atoms and from 0 to 2 additional heteroatomsselected from nitrogen, oxygen or sulfur, the ring system optionallybeing substituted with at least one halo, cyano, C₁-C₈alkyl, aryl,hetaryl, arylC₁-C₆alkyl, hetarylC₁-C₆alkyl, hydroxy, oxo, C₁-C₆alkyloxy,arylC₁-C₆alkyloxy, hetarylC₁-C₆alkyloxy, C₁-C₆alkyloxyC₁-C₆alkyl,C₁-C₆alkylcarbonyl, arylcarbonyl, hetarylcarbonyl,arylC₁-C₆alkylcarbonyl, hetarylC₁-C₆alkylcarbonyl, C₁-C₆alkylcarboxy,arylcarboxy, hetarylcarboxy, arylC₁-C₆alkylcarboxy orhetarylC₁-C₆alkylcarboxy.
 13. The method according to claim 3, whereinR¹⁵ is CONR⁸R⁹.
 14. The method according to claim 3, wherein R¹⁸ isC₁-C₆alkyl.
 15. The method according to claim 3, wherein the substitutedamide or a prodrug thereof of formula (I) is selected from the groupconsisting of:3-(10,11-Dihydro-dibenzo[b,f]azepin-5-yl)-1-[4-(1H-imidazol-4-yl)-piperidin-1-yl]-propan-1-one;4-(10,11-Dihydro-dibenzo[b,f]azepin-5-yl)-1-[4-(3H-imidazol-4-yl)-piperidin-1-yl]-butan-1-one;2,4-Bis-benzyloxy-benzamide; (1H-Indol-4-yl)-piperidin-1-yl-methanone;N-(1,4-Dioxo-1,4-dihydro-naphthalen-2-yl)-benzamide;N-(2,3-Dihydroxy-propyl)-2-(2-phenyl-adamantan-2-yl)-acetamide;(6-Fluoro-2-methyl-3,4-dihydro-2H-quinolin-1-yl)-phenyl-methanone;(2-Chloro-phenyl)-(6-fluoro-2-methyl-3,4-dihydro-2H-quinolin-1-yl)-methanone;3-Cyclopentyl-1-(6-fluoro-2-methyl-3,4-dihydro-2H-quinolin-1-yl)-propan-1-one;(3-Chloro-thieno[2,3-b]thiophen-2-yl)-thiomorpholin-4-yl-methanone;2-[2-(4-Chloro-phenyl)-adamantan-2-yl]-1-[4-(4-methoxy-phenyl)-piperazin-1-yl]-ethanone;1-(4-Benzyl-piperazin-1-yl)-2-[2-(4-chloro-phenyl)-adamantan-2-yl]-ethanone;2-[2-(4-Chloro-phenyl)-adamantan-2-yl]-1-(4-methyl-piperazin-1-yl)-ethanone;1-[4-(6-Chloro-pyridin-2-yl)-piperazin-1-yl]-2-(2-phenyl-adamantan-2-yl)-ethanone;4-Chloro-N-(1,7,7-trimethyl-bicyclo[2.2.1]hept-2-yl)-benzamide;3-Chloro-benzo[b]thiophene-2-carboxylic acid(2-cyano-ethyl)-cyclohexyl-amide;2-[2-(Bicyclo[2.2.1]hept-5-en-2-ylamino)-4-oxo-4,5-dihydro-thiazol-5-yl]-N-(2-chloro-phenyl)acetamide;[3-(4-sec-Butyl-phenoxy)-phenyl]-piperidin-1-yl-methanone;3-(6-Chloro-pyridin-2-yloxy)-N-ethyl-benzamide;N-Benzyl-2,4-dichloro-N-pyridin-2-yl-benzamide;2-[Benzoyl-(3-chloro-4-fluoro-phenyl)-amino]-propionic acid butyl ester;2-[Benzoyl-(3-chloro-4-fluoro-phenyl)-amino]-propionic acid pentylester; 3-(4-Fluoro-phenyl)-1-(4-phenyl-piperidin-1-yl)-but-2-en-1-one;N-(1,7,7-Trimethyl-bicyclo[2.2.1]hept-2-yl)-benzamide;1-(3-Cyclopentyl-propionyl)-piperidine-3-carboxylic acid ethyl ester;4-Phenyl-1-phenylacetyl-piperidine-4-carbonitrile;1-Octanoyl-4-phenyl-piperidine-4-carbonitrile;2,2-Dimethyl-1-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-propan-1-one;(4-Chloro-phenyl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone;N-[1-(4-Methanesulfonyl-phenyl)-ethyl]-N-(tetrahydro-furan-2-ylmethyl)-benzamide;2-(2-Amino-phenylsulfanyl)-1-(5-fluoro-2,3-dihydro-indol-1-yl)-ethanone;N-(1-Methyl-2,3-dihydro-1H-indol-5-ylmethyl)-N-(tetrahydro-furan-2-ylmethyl)-benzamide;1-Benzoyl-piperidine-2-carboxylic acid ethyl ester;N-(2-Chloro-phenyl)-2-(1,2,3,4-tetrahydro-isoquinolin-1-yl)-acetamide;(Decahydro-naphthalen-1-yl)-(4-methyl-piperazin-1-yl)-methanone;(4-Methyl-piperazin-1-yl)-(2-p-tolylsulfanyl-phenyl)-methanone;Adamantane-1-carboxylic acid(3-benzyloxy-2-ethyl-6-methyl-pyridin-4-yl)-amide;(6-Fluoro-2-methyl-3,4-dihydro-2H-quinolin-1-yl)-(3,4,5-trimethoxy-phenyl)-methanone;N-Bicyclo[2.2.1]hept-2-yl-3-cyclopentyl-propionamide;(2-Benzo[1,2,5]oxadiazol-5-yl-thiazol-4-yl)-piperidin-1-yl-methanone;Thiophene-2-carboxylic acid[4-(4-fluoro-phenyl)-4-hydroxy-butyl]-isopropyl-amide;N-Cyclohexyl-3-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-propionamide;2-[(Adamantane-1-carbonyl)-amino]-3-(1H-indol-3-yl)-propionic acidmethyl ester; Adamantane-1-carboxylic acid[3-(1H-benzoimidazol-2-ylsulfanyl)-5-nitro-phenyl]-amide;N-Benzyl-N-(1-cyclopropyl-ethyl)-4-fluoro-benzamide;Thiophene-2-carboxylic acid2-[2-(2-phenyl-adamantan-2-yl)-acetylamino]-ethyl ester;N-(4-Acetyl-phenyl)-2-(2-phenyl-adamantan-2-yl)-acetamide;2-[2-(4-Chloro-phenyl)-adamantan-2-yl]-N-(2-hydroxy-ethyl)-acetamide;(4-Benzoyl-piperidin-1-yl)-thiophen-2-yl-methanone;N-(2-Benzoyl-4-methyl-phenyl)-3-phenyl-acrylamide;N-(2-Benzoyl-4-methyl-phenyl)-2-fluoro-benzamide;Adamantane-1-carboxylic acid (4-ethoxy-benzothiazol-2-yl)-amide;Adamantane-1-carboxylic acid (5-benzoyl-4-phenyl-thiazol-2-yl)-amide;3-(2-Hydroxy-phenyl)-1,3-di-piperidin-1-yl-propan-1-one;N-(1-Methyl-2-phenyl-ethyl)-3-phenyl-propionamide;4-Oxo-4-piperidin-1-yl-butyric acid 4-tert-butyl-cyclohexyl ester;N-tert-Butyl-N-(4-methoxy-benzyl)-4-nitro-benzamide;{4-[(Adamantane-1-carbonyl)-amino]-phenoxy}-acetic acid;2-(4-Isobutyl-phenyl)-N-(1-phenyl-ethyl)-propionamide;Adamantane-1-carboxylic acid4-[(adamantane-1-carbonyl)-amino]-2,6-dimethyl-pyridin-3-yl ester;2-Phenyl-1-(3-phenyl-pyrrolidin-1-yl)-ethanone; Adamantane-1-carboxylicacid 4-[(adamantane-1-carbonyl)-amino]-2-ethyl-6-methyl-pyridin-3-ylester;N-(1,3-Dioxo-1,3-dihydro-isoindol-2-ylmethyl)-N-(4-hydroxy-phenyl)-benzamide;Biphenyl-4-yl-piperidin-1-yl-methanone;Azepan-1-yl-(3,5-dichloro-phenyl)-methanone;Azepan-1-yl-biphenyl-4-yl-methanone;Azepan-1-yl-(4-chloro-phenyl)-methanone;3-Heptylcarbamoyl-bicyclo[2.2.1]hept-5-ene-2-carboxylic acid;Adamantan-1-yl-azepan-1-yl-methanone;N,N-Dibenzyl-3,4-dimethoxy-benzamide;N-Benzyl-N-isopropyl-4-nitro-benzamide;N-[2-(1H-Indol-3-yl)-1-methyl-ethyl]-2-(4-isobutyl-phenyl)-propionamide;N-tert-Butyl-2-(4-isobutyl-phenyl)-propionamide; Adamantane-1-carboxylicacid (2-acetyl-phenyl)-amide;N-(1,3-Dioxo-1,3-dihydro-isoindol-2-ylmethyl)-N-(4-fluoro-phenyl)-benzamide;(Octahydro-quinolin-1-yl)-phenyl-methanone;(7-Hydroxy-octahydro-quinolin-1-yl)-phenyl-methanone;N-(1,3-Dioxo-1,3-dihydro-isoindol-2-ylmethyl)-N-p-tolyl-benzamide;N,N-Dibenzyl-4-methyl-benzamide;(2-Chloro-phenyl)-(2-methyl-piperidin-1-yl)-methanone;[4-Bromo-3-(piperidine-1-sulfonyl)-phenyl]-piperidin-1-yl-methanone;2-Chloro-N-(3,4-dimethyl-phenyl)-benzamide;1-Azepan-1-yl-2-(3,3-dimethyl-3,4-dihydro-2H-isoquinolin-1-ylidene)-ethanone;N-Cyclohexyl-4-(2,4-dichloro-phenoxy)-butyramide;N-Benzo[1,3]dioxol-5-yl-2-chloro-benzamide;(4-Benzyl-piperidin-1-yl)-(2-chloro-phenyl)-methanone;2-(Benzothiazol-2-ylsulfanyl)-N-cyclohexyl-acetamide;Cyclohexanecarboxylic acid(7,7-dimethyl-5-oxo-5,6,7,8-tetrahydro-quinazolin-2-yl)-amide;2,4-Dichloro-N-ethyl-N-o-tolyl-benzamide;(4-Benzyl-piperidin-1-yl)-(4-fluoro-phenyl)-methanone;N-Cyclohexyl-4-(2,4-dichloro-phenoxy)-N-methyl-butyramide;3-[2-(1,3-Dioxo-1,3-dihydro-isoindol-2-yl)-ethyl]-adamantane-1-carboxylicacid; Morpholin-4-yl-(3-p-tolyl-adamantan-1-yl)-methanone;N-Benzyl-2,4-dichloro-N-methyl-benzamide; Thiophene-2-carboxylic aciddibenzylamide; Azepan-1-yl-(2-bromo-phenyl)-methanone;(3,4-Dichloro-phenyl)-(4-methyl-piperidin-1-yl)-methanone;N,N-Dibenzyl-3,4-dichloro-benzamide;4-(2,4-Dichloro-phenoxy)-1-piperidin-1-yl-butan-1-one;N,N-Dibenzyl-2-fluoro-benzamide;(2-Chloro-phenyl)-piperidin-1-yl-methanone;2-Chloro-N-(3-trifluoromethyl-phenyl)-benzamide;N-Benzyl-N-ethyl-2-phenyl-acetamide;(3,4-Dihydro-2H-quinolin-1-yl)-p-tolyl-methanone; Thiophene-2-carboxylicacid benzyl-ethyl-amide; N-Adamantan-1-yl-2-dibenzylamino-acetamide;N-Cyclohexyl-2-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-3-phenyl-propionamide;Thiophene-2-carboxylic acid cycloheptylamide;N-Cyclohexyl-3-diethylsulfamoyl-4-methyl-benzamide;4-Benzoyl-N-methyl-N-phenyl-benzamide;N-Benzyl-2-bromo-N-methyl-benzamide;2-Chloro-N-methyl-N-phenyl-benzamide;4-Chloro-N-ethyl-N-o-tolyl-benzamide; N-Benzyl-4,N-dimethyl-benzamide;2-(4-Chloro-3,5-dimethyl-phenoxy)-N-cyclohexyl-N-methyl-acetamide;N-Benzyl-2-bromo-N-isopropyl-benzamide;3-(2-Chloro-phenyl)-N-cyclohexyl-N-methyl-acrylamide;N-Phenyl-N-(2,2,5-trimethyl-hex-4-enyl)-acetamide;N-m-Tolyl-N-(2,2,5-trimethyl-hex-4-enyl)-acetamide;(3-Chloro-benzo[b]thiophen-2-yl)-(4-methyl-piperazin-1-yl)-methanone;Adamantane-1-carboxylic acid (5-methyl-pyridin-2-yl)-amide;3-Bromo-N-[2-methyl-1-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]octane-6-carbonyl)-butyl]-benzamide;4-Chloro-N-[2-methyl-1-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]octane-6-carbonyl)-butyl]-benzamide;4-Methyl-N-[2-methyl-1-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]octane-6-carbonyl)-butyl]-benzamide;Cyclohexanecarboxylic acid[2-methyl-1-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]octane-6-carbonyl)butyl]-amide;3-Cyclopentyl-N-[2-methyl-1-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]octane-6-carbonyl)-butyl]-propionamide;2-Chloro-N-[2-(4-ethyl-benzoylamino)-ethyl]-N-(4-fluoro-phenyl)-benzamide;N-{1-Benzyl-2-[4-(3-cyclopentyl-propionyl)-piperazin-1-yl]-2-oxo-ethyl}-3-cyclopentyl-propionamide;N-Bicyclo[2.2.1]hept-5-en-2-ylmethyl-3-cyclopentyl-N-[2-(1H-indol-3-yl)-ethyl]-propionamide;N-Bicyclo[2.2.1]hept-5-en-2-ylmethyl-2,4-dichloro-N-[2-(1H-indol-3-yl)-ethyl]-benzamide;Naphthalene-2-carboxylic acid(2-oxo-azepan-3-yl)-thiophen-3-ylmethyl-amide;3,4,5-Trimethoxy-N-(4-methyl-benzyl)-N-[6-(pyridin-2-ylamino)-hexyl]-benzamide;3-Cyclopentyl-N-(4-methyl-benzyl)-N-[6-(pyridin-2-ylamino)-hexyl]-propionamide;N-(3,4-Dimethoxy-benzyl)-3-methoxy-N-[6-(pyridin-2-ylamino)-hexyl]-benzamide;N,N-Dimethyl-2-[3-(4-nitro-phenyl)-adamantan-1-yl]-acetamide;Adamantane-1-carboxylic acid[4-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-butyl]-p-tolyl-amide;2-(1,3-Dioxo-1,3-dihydro-isoindol-2-yl)-3-methyl-N-(2-trifluoromethyl-phenyl)-butyramide;2-(4-Chloro-2-methyl-phenoxy)-N-(2-trifluoromethyl-phenyl)-propionamide;4-(2,4-Dichloro-phenoxy)-1-[4-(4-fluoro-phenyl)-piperazin-1-yl]-butan-1-one;(3,4-Dihydro-2H-quinolin-1-yl)-[3-(piperidine-1-sulfonyl)-phenyl]-methanone;Acetic acid 4-(azepane-1-carbonyl)-phenyl ester;N-Adamantan-1-ylmethyl-benzamide;[3-(4-Nitro-phenyl)-adamantan-1-yl]-piperidin-1-yl-methanone;N-(1,1-Dimethyl-hexyl)-2-morpholin-4-yl-acetamide;Adamantyl-1-carboxylic acid (2-methoxy-ethyl)-amide;N-(4-Adamantan-1-yl-2-methyl-phenyl)-acetamide;3-p-Tolyl-adamantane-1-carboxylic acid (2,5-dichloro-phenyl)-amide;(3-Chloro-adamantan-1-yl)-pyrrolidin-1-yl-methanone;2-Amino-5-cyclohexylcarbamoyl-4-methyl-thiophene-3-carboxylic acid ethylester;N-(2-Chloro-phenyl)-2-{3-[(2-chloro-phenylcarbamoyl)-methyl]-adamantan-1-yl}-acetamide;3-p-Tolyl-adamantane-1-carboxylic acid (2,4-difluoro-phenyl)-amide;Adamantyl-1-carboxylic acid tert-butylamide;2-Adamantan-1-yl-N-tert-butyl-acetamide;N-Methyl-N-phenyl-4-(pyrrolidine-1-sulfonyl)-benzamide;N-(1-Adamantan-1-yl-ethyl)-2-fluoro-benzamide; Adamantane-1-carboxylicacid [2-(3,4-dimethoxy-phenyl)-ethyl]-amide; Adamantane-1-carboxylicacid dimethylamide; N-Benzyl-4-chloro-N-(1-cyclopropyl-vinyl)-benzamide;3,5-Dimethyl-adamantane-1-carboxylic acid benzylamide;2,4-Dichloro-N-cyclohexyl-N-(2-hydroxy-ethyl)-benzamide;N-Adamantan-1-yl-2,4-dichloro-N-ethyl-benzamide;2-[(3-p-Tolyl-adamantane-1-carbonyl)-amino]-propionic acid methyl ester;N-Adamantan-1-yl-3-morpholin-4-yl-propionamide;3-p-Tolyl-adamantane-1-carboxylic acid isopropylamide;N-Adamantan-1-yl-2-benzylamino-acetamide;N-Benzyl-2,4-dichloro-N-(1-cyclopropyl-ethyl)-5-methyl-benzamide;2-[(Adamantane-1-carbonyl)-amino]-benzoic acid ethyl ester;N-Benzyl-N-isopropyl-4-methyl-3-nitro-benzamide;(3,4-Dihydro-2H-quinolin-1-yl)-(2-fluoro-phenyl)-methanone;N-Ethyl-2-fluoro-N-phenyl-benzamide;2-Phenethyl-N-(2-trifluoromethyl-phenyl)-benzamide;1-(3,4-Dihydro-2H-quinolin-1-yl)-2-o-tolyloxy-ethanone;2-(1-Benzyl-1H-imidazol-2-ylsulfanyl)-N-cyclohexyl-acetamide;Cyclohexanecarboxylic acid (2-propoxy-phenyl)-amide;2-{3-[4-(2-Chloro-phenyl)-piperazin-1-yl]-3-oxo-propyl}-isoindole-1,3-dione;N-Cyclopentyl-2-(2,4-dichloro-phenoxy)-propionamide;Adamantane-1-carboxylic acid (2-trifluoromethyl-phenyl)-amide;(4-Chloro-3-nitro-phenyl)-(2,6-dimethyl-piperidin-1-yl)-methanone;4-(2-Ethyl-phenyl)-4-aza-tricyclo[5.2.2.0^(2,6)]undec-8-ene-3,5-dione;2-Phenyl-N-(2-trifluoromethyl-phenyl)-butyramide;N-Adamantan-1-yl-4-chloro-2-nitro-benzamide;3-p-Tolyl-adamantane-1-carboxylic acid (2,3-dimethyl-phenyl)-amide;N-Benzyl-3-methyl-4-p-tolyl-butyramide;N-(2-Cyclohex-1-enyl-ethyl)-2-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-propionamide;(4-tert-Butyl-phenyl)-(3,4-dihydro-1H-isoquinolin-2-yl)-methanone;2-[1-(4-Chloro-benzenesulfonyl)-1H-benzoimidazol-2-ylsulfanyl]-N-thiophen-2-ylmethyl-acetamide;2-Phenoxy-1-[4-(2-trifluoromethyl-benzyl)-piperazin-1-yl]-ethanone;Cyclohexanecarboxylic acid[5-(2-fluoro-benzylsulfanylmethyl)-[1,3,4]thiadiazol-2-yl]-amide;4-Methyl-2-phenyl-thiazole-5-carboxylic acid naphthalen-1-ylamide;4-Fluoro-N-[4-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]octane-6-carbonyl)-phenyl]-benzenesulfonamide;(3-Methoxy-phenyl)-(4-o-tolyl-piperazin-1-yl)-methanone;N-Adamantan-1-yl-3-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-propionamide;N-Cyclooctyl-2-methoxy-3-methyl-benzamide;2-[4-(2,3,3-Trimethyl-6-aza-bicyclo[3.2.1]octane-6-carbonyl)-phenyl]-isoindole-1,3-dione;(2,3-Diphenyl-quinoxalin-6-yl)-(2,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone;Adamantan-1-yl-(1,3,4,5-tetrahydro-pyrido[4,3-b]indol-2-yl)-methanone;N-{4-[1-(Naphthalene-2-sulfonyl)-piperidin-3-yl]-butyl}-N′-p-tolyl-oxalamide;N-Benzyl-N-(2-oxo-2-pyrrolidin-1-yl-ethyl)-benzenesulfonamide;(4-Amino-phenyl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone;1-[4-(4-Fluoro-phenyl)-piperazin-1-yl]-2-(2-isopropyl-5-methyl-phenoxy)-ethanone;Adamantane-1-carboxylic acid benzyl-pyridin-2-yl-amide;Adamantan-1-yl-piperidin-1-yl-methanone;Adamantan-1-yl-pyrrolidin-1-yl-methanone;(3,4-Dihydro-2H-quinolin-1-yl)-o-tolyl-methanone; Adamantyl-1-carboxylicacid benzylamide; Pyridine-2-carboxylic acid adamantan-2-ylamide;(3-Chloro-adamantan-1-yl)-piperidin-1-yl-methanone;Adamantan-1-yl-(4-methyl-piperidin-1-yl)-methanone;2-[3-(Azepane-1-carbonyl)-phenyl]-isoindole-1,3-dione;2-[3-(Piperidine-1-carbonyl)-phenyl]-isoindole-1,3-dione;4-(Benzyl-methanesulfonyl-amino)-N-furan-2-ylmethyl-benzamide;(4-Nitro-phenyl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone;1-Cyclohexyl-5-oxo-pyrrolidine-3-carboxylic acid(4-chloro-3-nitro-phenyl)-amide;N-(2-Chloro-phenyl)-2-(2-oxo-2-phenyl-ethylsulfanyl)-acetamide;3-(4-Hydroxy-phenyl)-N-isochroman-1-ylmethyl-3-phenyl-propionamide;(4-Ethoxy-phenyl)-(2-methyl-piperidin-1-yl)-methanone;1-Cyclohexyl-5-oxo-pyrrolidine-3-carboxylic acid(3-chloro-phenyl)-amide;N-[4-(Benzyl-isopropyl-sulfamoyl)-phenyl]-acetamide;N-(3,4-Dimethyl-phenyl)-N-[4-(piperidine-1-carbonyl)-benzyl]-methanesulfonamide;2-(5-Phenyl-1H-imidazol-2-ylsulfanyl)-N-(1,1,3,3-tetramethyl-butyl)-acetamide;2-(Benzothiazol-2-ylsulfanyl)-N-(1,1,3,3-tetramethyl-butyl)-acetamide;2-(Benzooxazol-2-ylsulfanyl)-N-(1,1,3,3-tetramethyl-butyl)-acetamide;2-(Naphthalen-2-ylcarbamoylmethylsulfanyl)-N-(1,1,3,3-tetramethyl-butyl)-acetamide;Acetic acid 4-(3,5-dimethyl-piperidine-1-carbonyl)-phenyl ester;[1-(4-Chloro-benzenesulfonyl)-piperidin-3-yl]-(octahydro-quinolin-1-yl)-methanone;(4-Fluoro-phenyl)-(3,4,4a,8a-tetrahydro-2H-quinolin-1-yl)-methanone;N-Adamantan-1-yl-2-ethoxy-acetamide;2-(2-Oxo-2-phenothiazin-10-yl-ethyl)-hexahydro-isoindole-1,3-dione;Adamantane-1-carboxylic acid (tetrahydro-furan-2-ylmethyl)-amide;2-Bromo-N-cycloheptyl-benzamide;Bicyclo[2.2.1]hept-2-yl-[4-(2-ethoxy-phenyl)-piperazin-1-yl]-methanone;N-Furan-2-ylmethyl-2-phenyl-2-phenylsulfanyl-acetamide;Adamantane-1-carboxylic acid benzyl-methyl-amide;1-(3,4-Dihydro-2H-quinolin-1-yl)-3-(4-fluoro-phenyl)-propenone;Adamantan-1-yl-(2,6-dimethyl-piperidin-1-yl)-methanone;4-Methyl-N-homoadamantyl-3-yl-benzamide;(3,5-Dimethyl-piperidin-1-yl)-(3-methyl-4-nitro-phenyl)-methanone;Quinoline-2-carboxylic acid cyclooctylamide; Adamantane-1-carboxylicacid [2-(2,4-dimethoxy-phenyl)-ethyl]-amide;(3,4-Dihydro-1H-isoquinolin-2-yl)-o-tolyl-methanone;(3,6-Dichloro-benzo[b]thiophen-2-yl)-(4-methyl-piperazin-1-yl)-methanone;3-(1-Benzyl-1H-imidazol-2-ylsulfanyl)-N-cyclohexyl-propionamide;Propionic acid 2-amino-4-methyl-5-p-tolylcarbamoyl-thiophen-3-yl ester;2-Cyclohexyl-N-(2,6-dimethyl-phenyl)-N-furan-2-ylmethyl-acetamide;(3-Methoxy-phenyl)-(2,2,4-trimethyl-4-phenyl-3,4-dihydro-2H-quinolin-1-yl)-methanone;1-[4-(2,3,3-Trimethyl-6-aza-bicyclo[3.2.1]octane-6-carbonyl)-phenyl]-pyrrolidine-2,5-dione;1-(3,4-Dihydro-2H-quinolin-1-yl)-2-(1-naphthalen-1-yl-1H-tetrazol-5-ylsulfanyl)-ethanone;[4-(2,3-Dimethyl-phenyl)-piperazin-1-yl]-o-tolyl-methanone;(4-Benzyl-piperidin-1-yl)-(4-methyl-3-nitro-phenyl)-methanone;N-(2-Cyano-phenyl)-2-(9-ethyl-9H-1,3,4,9-tetraaza-fluoren-2-ylsulfanyl)-acetamide;N-(2-Cyano-phenyl)-2-(9-methyl-9H-1,3,4,9-tetraaza-fluoren-2-ylsulfanyl)-acetamide;1-(Thiophene-2-carbonyl)-2,3-dihydro-1H-quinolin-4-one;(3-Chloro-6-nitro-benzo[b]thiophen-2-yl)-piperidin-1-yl-methanone;(4-Bromo-phenyl)-(3,5-dimethyl-piperidin-1-yl)-methanone;2-Morpholin-4-yl-N-(1-phenyl-cyclopentylmethyl)-acetamide;9-Oxo-9H-fluorene-1-carboxylic acid (3-methyl-butyl)-amide;[4-(2,5-Dimethyl-pyrrol-1-yl)-phenyl]-(4-methyl-piperidin-1-yl)-methanone;N-Cycloheptyl-3-diethylsulfamoyl-benzamide;(4-Methoxy-phenyl)-(3-phenyl-piperidin-1-yl)-methanone;3-Amino-N-cyclohexyl-N-methyl-benzamide;N-Ethyl-3,4-dimethyl-N-phenyl-benzamide;N-Benzyl-3,4,N-trimethyl-benzamide;(4-Fluoro-phenyl)-(3-phenyl-piperidin-1-yl)-methanone;[4-(2,3-Dimethyl-phenyl)-piperazin-1-yl]-(3-methoxy-phenyl)-methanone;Furan-2-carboxylic acid[4-(4-methyl-piperidine-1-sulfonyl)-phenyl]-amide;N-(2-Cyclohex-1-enyl-ethyl)-2-o-tolyloxy-acetamide;5-(2-Chloro-phenoxymethyl)-furan-2-carboxylic acid(1-bicyclo[2.2.1]hept-2-yl-ethyl)-amide;3-(2-Chloro-phenyl)-1-[4-(2,3-dimethyl-phenyl)-piperazin-1-yl]-propenone;N-[3-(Azepane-1-carbonyl)-phenyl]-benzamide;[3-(Piperidine-1-carbonyl)-pyrazol-1-yl]-o-tolyl-methanone;N-(1-Phenyl-cyclopentylmethyl)-2-piperidin-1-yl-propionamide;2-Morpholin-4-yl-N-(1-phenyl-cyclopentylmethyl)-propionamide;N-[4-(Azepane-1-sulfonyl)-phenyl]-2,2,2-trifluoro-acetamide;2,3-Dihydro-benzo[1,4]dioxine-6-carboxylic acid(1-adamantan-1-yl-ethyl)-amide;N-Adamantan-1-yl-2-(3-methoxy-phenoxy)-acetamide;3-Chloro-benzo[b]thiophene-2-carboxylic acid(2-cyano-ethyl)-phenyl-amide;[4-(4-Nitro-benzyl)-piperidin-1-yl]-phenyl-methanone;[4-(2-Nitro-benzyl)-piperidin-1-yl]-phenyl-methanone;3-[5-(4-Fluoro-phenyl)-furan-2-yl]-1-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-propenone;2-(3-Fluoro-benzoylamino)-4-methyl-5-(piperidine-1-carbonyl)-thiophene-3-carboxylicacid methyl ester;N-(2-Ethyl-phenyl)-2-(3-methyl-piperidin-1-yl)-acetamide;2-(2-Methoxy-benzoylamino)-4-methyl-5-(piperidine-1-carbonyl)-thiophene-3-carboxylicacid methyl ester; 1-Phenyl-cyclopentanecarboxylic acid(4-phenyl-tetrahydro-pyran-4-ylmethyl)-amide;4-(2,4-Dichloro-phenoxy)-1-(4-phenyl-piperazin-1-yl)-butan-1-one;Naphthalene-1-carboxylic acid cycloheptylamide;N-Indan-5-yl-2-methyl-3-nitro-benzamide;N-Cyclohexyl-3-(2,2,2-trifluoro-ethoxymethyl)-benzamide;2-Methoxy-N-(1-phenyl-cyclopentylmethyl)-benzamide;[5-(2,5-Dichloro-phenoxymethyl)-furan-2-yl]-(2,6-dimethyl-morpholin-4-yl)-methanone;[5-(2-Bromo-phenoxymethyl)-furan-2-yl]-(2-methyl-piperidin-1-yl)-methanone;5-(2-Methoxy-phenoxymethyl)-furan-2-carboxylic acid cycloheptylamide;(3,4-Dihydro-1H-isoquinolin-2-yl)-[1-(2-nitro-benzenesulfonyl)-piperidin-3-yl]-methanone;N-Cyclooctyl-2-(4-methoxy-phenoxy)-acetamide;N-(2,3-Dimethyl-phenyl)-4-[methyl-(toluene-4-sulfonyl)-amino]-butyramide;N-Phenyl-N-[4-(piperidine-1-carbonyl)-benzyl]-benzenesulfonamide;N-[4-(3,4-Dihydro-1H-isoquinoline-2-carbonyl)-benzyl]-N-(3,4-dimethyl-phenyl)-methanesulfonamide;2,3-Dihydro-benzo[1,4]dioxine-2-carboxylic acidbicyclo[2.2.1]hept-2-ylamide;4,5,6,7-Tetrahydro-benzo[b]thiophene-3-carboxylic acid cycloheptylamide;N-(2-Azepan-1-yl-2-oxo-ethyl)-N-benzyl-4-fluoro-benzenesulfonamide;1-(2,6-Dimethyl-morpholin-4-yl)-3,3-diphenyl-propan-1-one;N-Bicyclo[2.2.1]hept-2-yl-4-morpholin-4-ylmethyl-benzamide;[3-(2-Chloro-6-nitro-phenoxy)-phenyl]-piperidin-1-yl-methanone;N-Adamantan-1-yl-2-(4-methyl-quinolin-2-ylsulfanyl)-acetamide;Cyclohexanecarboxylic acid (2-phenylsulfanyl-phenyl)-amide;(4-Hydroxy-4-phenyl-octahydro-quinolin-1-yl)-phenyl-methanone;3-Cyclohexyl-N-(3-phenyl-propyl)-propionamide;2-[1-(2,5-Dimethyl-phenyl)-1H-tetrazol-5-ylsulfanyl]-N-isopropyl-N-phenyl-acetamide;N-{2-[4-(3,4-Dihydro-1H-isoquinoline-2-sulfonyl)-phenyl]-ethyl}-acetamide;N-Benzyl-N-[2-oxo-2-(4-phenyl-piperazin-1-yl)-ethyl]-benzenesulfonamide;[4-(2-Chloro-6-nitro-phenoxy)-phenyl]-piperidin-1-yl-methanone;N-Cycloheptyl-3-phenyl-propionamide;(3-Chloro-6-methyl-benzo[b]thiophen-2-yl)-piperidin-1-yl-methanone;N-Cycloheptyl-2,4-dimethoxy-benzamide;N-(3-Chloro-phenyl)-2-(8,11,11-trimethyl-3,4,6-triaza-tricyclo[6.2.1.0^(2,7)]undeca-2(7),3,5-trien-5-ylsulfanyl)-acetamide;N-(2-Nitro-phenyl)-2-(8,11,11-trimethyl-3,4,6-triaza-tricyclo[6.2.1.0^(2,7)]undeca-2(7),3,5-trien-5-ylsulfanyl)-acetamide;N-Phenyl-2-(8,11,11-trimethyl-3,4,6-triaza-tricyclo[6.2.1.0^(2,7)]undeca-2(7),3,5-trien-5-ylsulfanyl)acetamide;N-Ethyl-3-methyl-N-o-tolyl-benzamide;N-[5-(2,4-Dichloro-benzylsulfanyl)-[1,3,4]thiadiazol-2-yl]-2,2-dimethyl-propionamide;4-Bromo-1-ethyl-1H-pyrazole-3-carboxylic acid(2-methylsulfanyl-phenyl)-amide; 5-Benzoyl-furan-2-carboxylic aciddiisopropylamide;N-{2-[2-(4-Bromo-phenyl)-2-oxo-ethylsulfanyl]-benzothiazol-6-yl}-acetamide;2-(6-Amino-benzothiazol-2-ylsulfanyl)-N-cyclohexyl-acetamide;N-(2-Cyclohexylcarbamoylmethylsulfanyl-benzothiazol-6-yl)-2-methoxy-benzamide;Benzofuran-2-yl-(4-phenyl-piperidin-1-yl)-methanone;1-(2-Nitro-phenyl)-piperidine-3-carboxylic acid diethylamide;1-(4-Nitro-phenyl)-piperidine-3-carboxylic acid diethylamide;5-Bromo-furan-2-carboxylic acid adamantan-2-ylamide;3,3-Dimethyl-pentanedioic acid bis-[(2,4-difluoro-phenyl)-amide];2-(3-Bromo-benzylsulfanyl)-1-(4-phenyl-piperazin-1-yl)-ethanone;N-(2-Azepan-1-yl-2-oxo-ethyl)-N-benzyl-4-bromo-benzenesulfonamide;1-(2,3-Dihydro-indol-1-yl)-2-p-tolylsulfanyl-ethanone;[4-(4-Bromo-benzenesulfonyl)-piperazin-1-yl]-furan-2-yl-methanone;[5-(2-Bromo-phenoxymethyl)-furan-2-yl]-(2,6-dimethyl-morpholin-4-yl)-methanone;5-(2-Chloro-phenoxymethyl)-furan-2-carboxylic acid diethylamide;5-(2-Bromo-phenoxymethyl)-furan-2-carboxylic acid diethylamide;5-(2-Chloro-phenoxymethyl)-furan-2-carboxylic acid methyl-phenyl-amide;[5-(2-Chloro-phenoxymethyl)-furan-2-yl]-(4-methyl-piperidin-1-yl)-methanone;[3-(2,5-Dichloro-phenoxymethyl)-phenyl]-pyrrolidin-1-yl-methanone;[5-(4-Ethoxy-phenoxymethyl)-furan-2-yl]-(4-methyl-piperidin-1-yl)-methanone;3-(1,3-Dioxo-1,3-dihydro-isoindol-2-yl)-N-(2-methyl-cyclohexyl)-propionamide;3-(3,4-Dihydro-2H-quinoline-1-carbonyl)-N-phenyl-benzenesulfonamide;[3-(2,3-Dihydro-indole-1-sulfonyl)-phenyl]-(3,4-dihydro-2H-quinolin-1-yl)-methanone;[3-(2,5-Dimethyl-pyrrol-1-yl)-phenyl]-(4-methyl-piperidin-1-yl)-methanone;N-Cyclohexyl-3-(2-hydroxy-4-methyl-phenyl)-3-phenyl-propionamide;2-Diethylamino-N-(1-phenyl-cyclopentylmethyl)-propionamide;(6-Fluoro-2-methyl-3,4-dihydro-2H-quinolin-1-yl)-(3-trifluoromethyl-phenyl)-methanone;(2,6-Dimethyl-morpholin-4-yl)-[4-(naphthalen-1-yloxymethyl)-phenyl]-methanone;N-Benzyl-4-bromo-N-ethyl-benzamide;(3-Methyl-piperidin-1-yl)-[4-(naphthalen-1-yloxymethyl)-phenyl]-methanone;Azepan-1-yl-[5-(2-chloro-phenoxymethyl)-furan-2-yl]-methanone;(4-Methyl-piperidin-1-yl)-[4-(naphthalen-1-yloxymethyl)-phenyl]-methanone;Azepan-1-yl-[5-(2,4-dichloro-phenoxymethyl)-furan-2-yl]-methanone;N-Cycloheptyl-4-(4-methoxy-2-methyl-phenyl)-butyramide;2-(4-Benzothiazol-2-yl-piperazin-1-yl)-N-cyclohexyl-acetamide;N-Cycloheptyl-2-(2,6-dimethyl-phenoxy)-acetamide;(3,4-Dihydro-2H-quinolin-1-yl)-(3-iodo-phenyl)-methanone;N-Cycloheptyl-3-(2,2,2-trifluoro-ethoxymethyl)-benzamide;Azepan-1-yl-[4-(2-chloro-phenoxymethyl)-phenyl]-methanone;(2,6-Dimethyl-morpholin-4-yl)-[4-(naphthalen-2-yloxymethyl)-phenyl]-methanone;Azepan-1-yl-[3-(4-ethoxy-phenoxymethyl)-phenyl]-methanone;Benzo[b]thiophene-3-carboxylic acid(1,2,3,4-tetrahydro-naphthalen-1-yl)-amide;2-(4-Chloro-2-methyl-phenoxy)-N-cycloheptyl-acetamide;2,4-Dichloro-N-cyclohexyl-N-methyl-benzamide;N-Cyclooctyl-2-p-tolyloxy-acetamide;(3,5-Dimethyl-piperidin-1-yl)-(4-methyl-3-nitro-phenyl)-methanone;Biphenyl-4-yl-(2,6-dimethyl-piperidin-1-yl)-methanone;N-Cyclohexyl-4-fluoro-N-methyl-benzamide;N-[4-(Azepane-1-carbonyl)-phenyl]-N-methyl-benzenesulfonamide;N-Cycloheptyl-2-fluoro-benzamide; N-Cycloheptyl-4-methyl-benzamide;(3-Methyl-piperidin-1-yl)-p-tolyl-methanone;[2-(3,4-Dimethoxy-phenylcarbamoyl)-piperidin-1-yl]-acetic acid benzylester; N-[4-(2-Methyl-piperidine-1-sulfonyl)-phenyl]-acetamide;2-(2,4-Dichloro-phenoxy)-N-(2-methyl-butyl)-propionamide;[4-(2-Chloro-6-nitro-phenyl)-piperazin-1-yl]-(4-methoxy-phenyl)-methanone;N-Cyclohexyl-4-(4-methoxy-3-methyl-phenyl)-butyramide;(3-Chloro-6-methoxy-benzo[b]thiophen-2-yl)-(3,4-dihydro-1H-isoquinolin-2-yl)-methanone;2-(4-Methyl-benzylsulfanyl)-1-piperidin-1-yl-ethanone;N-Cyclohexyl-N-[(4-phenyl-thiazol-2-ylcarbamoyl)-methyl]-benzamide;N-(2-Azepan-1-yl-2-oxo-ethyl)-N-(4-isopropyl-phenyl)-methanesulfonamide;N-Adamantan-1-yl-3-p-tolylsulfanyl-propionamide;6-(2,4-Dichloro-phenylcarbamoyl)-3,4-dimethyl-cyclohex-3-enecarboxylicacid; (4-Butyl-cyclohexyl)-morpholin-4-yl-methanone;(3,4-Dichloro-phenyl)-(3,4-dihydro-2H-quinolin-1-yl)-methanone;N-(2-Cyclohex-1-enyl-ethyl)-3-methoxy-benzamide;N-Adamantan-2-yl-3-(1,5-dimethyl-1H-pyrazol-4-yl)-acrylamide;N-Adamantan-1-yl-N-methyl-4-(4-nitro-pyrazol-1-ylmethyl)-benzamide;5-(4-Chloro-3,5-dimethyl-pyrazol-1-ylmethyl)-furan-2-carboxylic acidadamantan-2-ylamide;2-(4-Chloro-phenoxy)-N-(2-fluoro-5-methyl-phenyl)-2-methyl-propionamide;N-Adamantan-1-yl-2-(4-chloro-3,5-dimethyl-phenoxy)-acetamide;2-[(3-Carboxy-bicyclo[2.2.1]heptane-2-carbonyl)-amino]-5,6-dihydro-4H-cyclopenta[b]thiophene-3-carboxylicacid propyl ester;2-Adamantan-1-yl-N-[1-(2,5-dimethyl-phenyl)-ethyl]-acetamide;3-Methyl-thiophene-2-carboxylic acid cyclooctylamide;N-p-Tolyl-2-(8,11,11-trimethyl-3,4,6-triaza-tricyclo[6.2.1.0^(2,7)]undeca-2,4,6-trien-5-ylsulfanyl)propionamide;Azepan-1-yl-[5-(4-chloro-5-methyl-3-nitro-pyrazol-1-ylmethyl)-furan-2-yl]-methanone;N-Adamantan-2-yl-3-(4-bromo-3-nitro-pyrazol-1-ylmethyl)-benzamide;N-Bicyclo[2.2.1]hept-2-yl-2-chloro-benzamide;[5-(3-Chloro-phenoxymethyl)-furan-2-yl]-piperidin-1-yl-methanone;1-(4-Ethyl-benzoyl)-6-methoxy-2-methyl-2,3-dihydro-1H-quinolin-4-one;6-Fluoro-2-methyl-1-{3-[4-(propane-1-sulfonyl)-phenoxymethyl]-benzoyl}-2,3-dihydro-1H-quinolin-4-one;N-Cycloheptyl-2-(naphthalen-1-yloxy)-acetamide;N-Cyclohexyl-4-o-tolyloxy-butyramide;(2-Benzylsulfanyl-phenyl)-morpholin-4-yl-methanone;(2-Chloro-5,6-difluoro-3-methyl-phenyl)-(4-methyl-piperidin-1-yl)-methanone;(3-Bromo-phenyl)-[4-(4-chloro-2-nitro-phenyl)-piperazin-1-yl]-methanone;2-Bromo-N-(1,1,3,3-tetramethyl-butyl)-benzamide;N-Adamantan-1-yl-2-(2-benzoyl-5-methoxy-phenoxy)-acetamide;N-Cyclohexyl-3-methyl-4-p-tolyl-butyramide;[5-(4-Methyl-2-nitro-phenoxymethyl)-furan-2-yl]-thiomorpholin-4-yl-methanone;[5-(2,5-Dichloro-phenoxymethyl)-furan-2-yl]-thiomorpholin-4-yl-methanone;5-(4-Chloro-2-nitro-phenoxymethyl)-furan-2-carboxylic acidadamantan-1-ylamide; 4,5,6,7-Tetrahydro-benzo[b]thiophene-3-carboxylicacid cyclohexylamide; 4-Chloro-1,5-dimethyl-1H-pyrazole-3-carboxylicacid adamantan-1-yl-methyl-amide;4-(4-Methoxy-3-methyl-phenyl)-N-(2-methyl-cyclohexyl)-butyramide;3-Benzo[1,3]dioxol-5-yl-1-(3,4-dihydro-1H-isoquinolin-2-yl)-propenone;N-Bicyclo[2.2.1]hept-2-yl-3-phenylsulfanyl-propionamide;Azepan-1-yl-[5-(2-nitro-phenoxymethyl)-furan-2-yl]-methanone;N-Benzyl-2-(4-chloro-phenylsulfanyl)-N-methyl-acetamide;1-(4-Benzyl-piperidin-1-yl)-2-benzylsulfanyl-ethanone;2-(4-tert-Butyl-phenoxy)-1-(4-ethyl-piperazin-1-yl)-ethanone;[4-(4-Ethoxy-phenoxymethyl)-phenyl]-(4-methyl-piperidin-1-yl)-methanone;5-(4-Bromo-3,5-dimethyl-pyrazol-1-ylmethyl)-furan-2-carboxylic acidadamantan-2-ylamide;1-Azepan-1-yl-3-(4-chloro-phenylsulfanyl)-propan-1-one;N-Bicyclo[2.2.1]hept-2-yl-2-(2-chloro-benzylsulfanyl)-acetamide;2-(2-Methyl-benzylsulfanyl)-1-(4-phenyl-piperazin-1-yl)-ethanone;N-[2-(1-Benzo[1,3]dioxol-5-yl-3-furan-2-yl-3-oxo-propylsulfanyl)-phenyl]-acetamide;(3,5-Dimethyl-piperidin-1-yl)-(3-iodo-phenyl)-methanone;[5-(2-Bromo-phenoxymethyl)-furan-2-yl]-(6-fluoro-2-methyl-3,4-dihydro-2H-quinolin-1-yl)-methanone;N-Benzyl-N-cyclohex-1-enyl-isonicotinamide;1-[4-(4-Fluoro-phenyl)-piperazin-1-yl]-2-(2-methyl-benzylsulfanyl)-ethanone;2-(2-Bromo-4-methyl-phenoxy)-N-(2-cyclohex-1-enyl-ethyl)-acetamide;2-[5-(2-Hydroxy-phenyl)-[1,3,4]oxadiazol-2-ylsulfanyl]-1-piperidin-1-yl-ethanone;5-(4-Nitro-pyrazol-1-ylmethyl)-furan-2-carboxylic acidadamantan-2-ylamide;3-Benzo[1,3]dioxol-5-yl-3-(2-methoxy-phenyl)-1-pyrrolidin-1-yl-propan-1-one;N-Adamantan-2-yl-3,4-dichloro-benzamide;Benzo[b]thiophen-3-yl-(6-fluoro-2-methyl-3,4-dihydro-2H-quinolin-1-yl)-methanone;2-Adamantan-1-yl-1-(3,4-dihydro-1H-isoquinolin-2-yl)-ethanone;4,5,6,7-Tetrahydro-benzo[b]thiophene-3-carboxylic acid(2-cyclohex-1-enyl-ethyl)-amide; Benzo[b]thiophene-3-carboxylic acid(3,3,5-trimethyl-cyclohexyl)-amide;2-(2,6-Dimethyl-phenoxy)-N-(2-isopropyl-phenyl)-acetamide;4-Bromo-N-[3-(piperidine-1-carbonyl)-phenyl]-benzamide;N-Benzo[1,3]dioxol-5-ylmethyl-2-(2-cyano-phenylsulfanyl)-benzamide;N-Adamantan-1-yl-2-(naphthalen-2-yloxy)-acetamide;[4-(4-Chloro-phenylsulfanylmethyl)-phenyl]-morpholin-4-yl-methanone;Thiophene-2-carboxylic acid (3,3,5-trimethyl-cyclohexyl)-amide;Benzo[1,3]dioxol-5-yl-(3,4-dihydro-2H-quinolin-1-yl)-methanone;3-Chloro-benzo[b]thiophene-2-carboxylic acid cyclooctylamide;2-[2-Morpholin-4-yl-1-(4-nitro-benzyl)-2-oxo-ethyl]-isoindole-1,3-dione;2-Hydroxy-4,4-dimethyl-6-oxo-cyclohex-1-enecarboxylic acid phenylamide;(2,4-Dichloro-phenyl)-(2,6-dimethyl-piperidin-1-yl)-methanone;Adamantane-1-carboxylic acid furan-2-ylmethyl-p-tolyl-amide;Azocan-1-yl-(4-tert-butyl-phenyl)-methanone;3-Chloro-benzo[b]thiophene-2-carboxylic acid benzyl-methyl-amide;Adamantane-1-carboxylic acid (2-fluoro-phenyl)-amide;2-(Piperidine-1-carbonyl)-5-piperidin-1-yl-oxazole-4-carbonitrile;N-(4,6-Dimethyl-5-nitro-pyridin-3-yl)-benzamide;Adamantan-1-yl-[4-(2-methoxy-phenyl)-piperazin-1-yl]-methanone;(2-Methyl-piperidin-1-yl)-o-tolyl-methanone;N-Benzyl-4-chloro-N-isopropyl-3-nitro-benzamide;N-(3-Hexylsulfanyl-[1,2,4]thiadiazol-5-yl)-3-methyl-butyramide; 4,N-Dimethyl-N-[4-(piperidine-1-carbonyl)-phenyl]-benzenesulfonamide;Azepan-1-yl-(5-tert-butyl-2H-pyrazol-3-yl)-methanone;2-Amino-4-methyl-5-(piperidine-1-carbonyl)-thiophene-3-carboxylic acidethyl ester; 5-Methyl-furan-2-carboxylic acid(1-adamantan-1-yl-ethyl)-amide;(3-Chloro-6-methyl-benzo[b]thiophen-2-yl)-(3,4-dihydro-1H-isoquinolin-2-yl)-methanone;N-Adamantan-1-yl-2-trifluoromethyl-benzamide;(3-Bromo-phenyl)-(2,2,4-trimethyl-4-phenyl-3,4-dihydro-2H-quinolin-1-yl)-methanone;Benzo[1,3]dioxole-5-carboxylic acid dipropylamide;N-(3,3-Diphenyl-propyl)-4-methoxy-benzamide;[4-(2-Chloro-6-nitro-phenyl)-piperazin-1-yl]-p-tolyl-methanone;Furan-2-yl-[4-(toluene-4-sulfonyl)-piperazin-1-yl]-methanone;3-(2-Chloro-6-fluoro-phenyl)-1-(3,4-dihydro-2H-quinolin-1-yl)-propenone;2-Chloro-N-cycloheptyl-benzamide;1-[4-(4-Nitro-phenyl)-piperazin-1-yl]-3-phenyl-propan-1-one;(3,4-Dihydro-1H-isoquinolin-2-yl)-(3,4-dimethyl-phenyl)-methanone;(1-Adamantan-1-yl-4-bromo-1H-pyrazol-3-yl)-morpholin-4-yl-methanone;2-Phenyl-cyclopropanecarboxylic acid cyclooctylamide;3-[4-(2-Ethoxy-phenyl)-piperazine-1-carbonyl]-isochromen-1-one;[3-(4-Bromo-pyrazol-1-ylmethyl)-phenyl]-(4-methyl-piperidin-1-yl)-methanone;2-Azepan-1-yl-N-biphenyl-2-yl-acetamide;N-[5-(3,4-Dimethoxy-benzyl)-[1,3,4]thiadiazol-2-yl]-3-methyl-butyramide;Adamantan-1-yl-(4-phenyl-piperidin-1-yl)-methanone;N-(2-Azepan-1-yl-2-oxo-ethyl)-N-(4-ethoxy-phenyl)-4-methylsulfanyl-benzenesulfonamide;1-Adamantan-1-yl-4-bromo-1H-pyrazole-3-carboxylic acid diethylamide;(6-Fluoro-2-methyl-3,4-dihydro-2H-quinolin-1-yl)-(2-fluoro-phenyl)-methanone;3-[4-(2,3-Dimethyl-phenyl)-piperazine-1-carbonyl]-isochromen-1-one;N-Cyclooctyl-2-(2-methoxy-phenoxy)-acetamide;N-Cyclohexyl-N-methyl-2-nitro-benzamide; Adamantane-1-carboxylic acid(1,1-dioxo-tetrahydro-thiophen-3-yl)-amide;N-Adamantan-2-yl-2-(4-chloro-phenyl)-acetamide;(2,4-Dichloro-phenyl)-(3-methyl-piperidin-1-yl)-methanone;2-(4-tert-Butyl-phenoxy)-N-cyclooctyl-acetamide;(10,11-Dihydro-dibenzo[b,f]azepin-5-yl)-(2-methoxy-phenyl)-methanone;(3-Chloro-phenyl)-(2-methyl-piperidin-1-yl)-methanone;(3-Chloro-6-nitro-benzo[b]thiophen-2-yl)-(3-methyl-piperidin-1-yl)-methanone;(2,5-Dichloro-phenyl)-(4-methyl-piperidin-1-yl)-methanone;N-[5-(3,4-Dichloro-benzyl)-[1,3,4]thiadiazol-2-yl]-2,2-dimethyl-propionamide;4-(4-Chloro-2-methyl-phenoxy)-1-(3,4-dihydro-2H-quinolin-1-yl)-butan-1-one;(3,4-Dichloro-phenyl)-[4-(2,3-dimethyl-phenyl)-piperazin-1-yl]-methanone;Cyclooctanecarboxylic acid[1-(naphthalene-2-sulfonyl)-pyrrolidin-2-yl]-amide;1-Butyl-pyrrolidine-2-carboxylic acid benzo[1,3]dioxol-4-ylamide;5-Methyl-furan-2-carboxylic acid dibenzylamide;(3,4-Dihydro-2H-quinolin-1-yl)-[3-(4-phenyl-piperazine-1-sulfonyl)-phenyl]-methanone;Bicyclo[2.2.1]hept-2-yl-[4-(2,3-dimethyl-phenyl)-piperazin-1-yl]-methanone;N-Adamantan-1-yl-2-benzoyl-benzamide;[5-(2-Chloro-phenoxymethyl)-furan-2-yl]-(3-methyl-piperidin-1-yl)-methanone;(3,5-Dimethyl-piperidin-1-yl)-(2-iodo-phenyl)-methanone;1-Benzenesulfonyl-pyrrolidine-2-carboxylic acid cyclooctylamide;(3,4-Dimethoxy-phenyl)-(6-fluoro-2-methyl-3,4-dihydro-2H-quinolin-1-yl)-methanone;3-(2,6-Dichloro-phenyl)-1-(2-ethyl-piperidin-1-yl)-propenone;N-(3,4-Difluoro-phenyl)-2,6-difluoro-benzamide;2,6-Difluoro-N-naphthalen-1-yl-benzamide;(4-Chloro-phenyl)-(3,5-dimethyl-piperidin-1-yl)-methanone;N-[4-(2,6-Dimethyl-piperidine-1-carbonyl)-phenyl]-2-(naphthalen-2-yloxy)-acetamide;(2-Chloro-phenyl)-(3-methyl-piperidin-1-yl)-methanone;N-{2-[4-(Piperidine-1-sulfonyl)-phenyl]-ethyl}-acetamide;N-Biphenyl-2-yl-2-(pyridin-2-ylsulfanyl)-acetamide;Azepan-1-yl-[5-(4-chloro-3,5-dimethyl-pyrazol-1-ylmethyl)-furan-2-yl]-methanone;Acetic acid 4-(4-methyl-piperidine-1-carbonyl)-phenyl ester; Acetic acid4-(4-benzyl-piperidine-1-carbonyl)-phenyl ester;Benzo[1,3]dioxole-5-carboxylic acid cycloheptylamide;2-(2,4-Dimethyl-phenoxy)-1-(6-fluoro-2-methyl-3,4-dihydro-2H-quinolin-1-yl)-ethanone;Acetic acid 4-(3,4-dihydro-2H-quinoline-1-carbonyl)-phenyl ester;Azepan-1-yl-(3,5-dibromo-phenyl)-methanone;(3,5-Dibromo-phenyl)-[4-(2-methoxy-phenyl)-piperazin-1-yl]-methanone;N-Cyclooctyl-4-isopropyl-benzamide;N-Cyclooctyl-2-(4-methoxy-phenyl)-acetamide;(4-tert-Butyl-piperidin-1-yl)-phenyl-methanone;N-(4-tert-Butyl-3-nitro-phenyl)-acetamide;(2,6-Dimethyl-piperidin-1-yl)-[5-(2,3,5,6-tetrafluoro-phenoxymethyl)-furan-2-yl]-methanone;N-Cyclohexyl-3-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-N-methyl-propionamide;2-(4-Chloro-3-methyl-phenoxy)-N-cyclohexyl-N-methyl-acetamide;N-Cyclopentyl-3-(3,4-dihydro-2H-quinoline-1-carbonyl)-benzenesulfonamide;(3,4-Dihydro-1H-isoquinolin-2-yl)-(3-dimethylamino-phenyl)-methanone;3-Cyclohexylcarbamoyl-bicyclo[2.2.1]hept-5-ene-2-carboxylic acidisopropyl ester;1-(3,4-Dihydro-1H-isoquinolin-2-yl)-2-(2-methoxy-phenyl)-ethanone;N-Benzyl-N-cyclohex-1-enyl-benzamide;[1-(Thiophene-2-sulfonyl)-piperidin-4-yl]-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone;N-Adamantan-1-yl-2-(1-phenyl-1H-tetrazol-5-ylsulfanyl)-acetamide;(3,4-Dihydro-2H-quinolin-1-yl)-[4-(morpholine-4-sulfonyl)-phenyl]-methanone;(3,4-Dihydro-2H-quinolin-1-yl)-[4-(pyrrolidine-1-sulfonyl)-phenyl]-methanone;(3,4-Dihydro-2H-quinolin-1-yl)-[1-(thiophene-2-sulfonyl)-piperidin-4-yl]-methanone;(1-Benzenesulfonyl-piperidin-3-yl)-(3,4-dihydro-1H-isoquinolin-2-yl)-methanone;6,7-Dimethyl-4-oxa-tricyclo[4.3.0.0^(3,7)]nonane-3-carboxylic acidcyclohexylamide;6,7-Dimethyl-4-oxa-tricyclo[4.3.0.0^(3,7)]nonane-3-carboxylic acid(2-chloro-phenyl)-amide;(6,7-Dimethyl-4-oxa-tricyclo[4.3.0.0^(3,7)]non-3-yl)-piperidin-1-yl-methanone;2-(5,6-Dimethyl-4-oxo-3,4-dihydro-thieno[2,3-d]pyrimidin-2-ylsulfanyl)-N-furan-2-ylmethyl-acetamide;N-Allyl-2-(5,6-dimethyl-4-oxo-3,4-dihydro-thieno[2,3-d]pyrimidin-2-ylsulfanyl)-acetamide;N-Adamantan-1-yl-2-(5,6,7,8-tetrahydro-benzo[4,5]thieno[2,3-d]pyrimidin-4-ylsulfanyl)-acetamide;1-(3,4-Dihydro-2H-quinoline-1-carbonyl)-4,7,7-trimethyl-2-oxa-bicyclo[2.2.1]heptan-3-one;1-(3,4-Dihydro-1H-isoquinoline-2-carbonyl)-4,7,7-trimethyl-2-oxa-bicyclo[2.2.1]heptan-3-one;Azepan-1-yl-(6,7-dimethyl-4-oxa-tricyclo[4.3.0.0^(3,7)]non-3-yl)-methanone;2,5-Dimethyl-furan-3-carboxylic acid (1-adamantan-1-yl-ethyl)-amide;1-Cyclohexyl-5-oxo-pyrrolidine-3-carboxylic acid(3-cyano-4,5,6,7-tetrahydro-benzo[b]thiophen-2-yl)-amide;2-(2-Cyano-phenylsulfanyl)-N-cyclopentyl-benzamide;[5-(2-Methoxy-4-propyl-phenoxymethyl)-furan-2-yl]-(3-methyl-piperidin-1-yl)-methanone;(4-tert-Butyl-phenyl)-(3,5-dimethyl-piperidin-1-yl)-methanone;[4-(2-Methoxy-naphthalen-1-ylmethyl)-piperazin-1-yl]-(4-methoxy-phenyl)-methanone;(3,4-Dichloro-phenyl)-(3,5-dimethyl-piperidin-1-yl)-methanone;(4-Ethoxy-phenyl)-(4-methyl-piperidin-1-yl)-methanone;2-Phenethyl-N-(tetrahydro-furan-2-ylmethyl)-benzamide;N-Cycloheptyl-2-phenoxy-benzamide; Adamantane-1-carboxylic acid(2-ethoxy-phenyl)-amide; N-Adamantan-2-yl-2-o-tolyloxy-acetamide;(2-Chloro-phenyl)-(3,5-dimethyl-piperidin-1-yl)-methanone;1-Morpholin-4-yl-2-[3-(4-nitro-phenyl)-adamantan-1-yl]-ethanone;2-Dimethylamino-N-(2-nitro-phenyl)-benzamide;N-Benzyl-2-(4,4,6-trimethyl-1-p-tolyl-1,4-dihydro-pyrimidin-2-ylsulfanyl)-acetamide;[4-(3,5-Dinitro-phenoxy)-phenyl]-(2-ethyl-piperidin-1-yl)-methanone;1-(4-Chloro-benzoyl)-2,3-dihydro-1H-benzo[g]quinolin-4-one;2-[(Adamantane-1-carbonyl)-amino]-3-phenyl-propionic acid methyl ester;[Benzyl-(4-nitro-benzoyl)-amino]-acetic acid ethyl ester;9-Oxo-9H-fluorene-3-carboxylic acid methyl-(4-nitro-phenyl)-amide;Adamantane-1-carboxylic acid [2-(4-methoxy-phenyl)-ethyl]-amide;(10,11-Dihydro-dibenzo[b,f]azepin-5-yl)-(4-fluoro-phenyl)-methanone;2-Benzylsulfanyl-N-[2-(2-methoxy-phenoxy)-ethyl]-acetamide;N-Adamantan-1-yl-2-(2-oxo-4-phenyl-pyrrolidin-1-yl)-acetamide;2-Bromo-N-tricyclo[3.2.1.0^(2,4)]oct-6-ylmethyl-benzamide;Adamantane-1-carboxylic acid (2,6-dimethoxy-pyrimidin-4-yl)-amide;Hexanedioic acid(2,7,7-trimethyl-bicyclo[2.2.1]hept-1-yl)-amide(1,7,7-trimethyl-bicyclo[2.2.1]hept-2-yl)-amide;2-Chloro-N-(2-cyclohexyl-ethyl)-benzamide;2-[3-(2-Ethyl-piperidin-1-yl)-3-oxo-propyl]-isoindole-1,3-dione;N-Adamantan-1-yl-2-hydroxy-2,2-diphenyl-acetamide;Adamantane-1-carboxylic acid (naphthalen-1-ylmethyl)-amide;Adamantane-1-carboxylic acid (benzo[1,3]dioxol-5-ylmethyl)-amide;1-(Azepane-1-carbonyl)-fluoren-9-one;2-(Quinolin-2-ylsulfanyl)-N-p-tolyl-acetamide;2,4-Dichloro-N-[3-(piperidine-1-carbonyl)-phenyl]-benzamide;2-Chloro-4,5-difluoro-N-(3,3,5-trimethyl-cyclohexyl)-benzamide;2-(2-Chloro-benzylsulfanyl)-N-p-tolyl-acetamide;[4-(4-Chloro-phenylsulfanylmethyl)-phenyl]-pyrrolidin-1-yl-methanone;N-Adamantan-1-yl-N-methyl-isonicotinamide;Azepan-1-yl-[4-(4-chloro-phenylsulfanylmethyl)-phenyl]-methanone;(2-Chloro-phenyl)-(1,5,7-trimethyl-3,7-diaza-bicyclo[3.3.1]non-3-yl)-methanone;(3-Chloro-benzo[b]thiophen-2-yl)-(4-methyl-piperidin-1-yl)-methanone;Benzoic acid 1-benzoyl-decahydro-quinolin-4-yl ester;2-(3-Bromo-benzylsulfanyl)-1-[4-(2-methoxy-phenyl)-piperazin-1-yl]-ethanone;4-Methyl-N-[2-(phenoxazine-10-carbonyl)-phenyl]-benzenesulfonamide;2-[1-(Azepane-1-carbonyl)-2-methyl-propyl]-isoindole-1,3-dione;2-(3-Bromo-benzylsulfanyl)-1-piperidin-1-yl-ethanone;1-[3-(4-Bromo-phenyl)-1-furan-2-yl-3-oxo-propyl]-pyrrolidin-2-one;2-Chloro-N-cyclooctyl-4,5-difluoro-benzamide;2,4-Dichloro-N-(2-furan-2-ylmethyl-cyclohexyl)-benzamide;N-(4-Benzoyl-furazan-3-yl)-2-fluoro-benzamide;N-Adamantan-1-yl-2-(3-cyano-4-methoxymethyl-6-methyl-pyridin-2-ylsulfany)-acetamide;4-tert-Butyl-N-cyclooctyl-benzamide;N-Adamantan-1-yl-2-phenyl-butyramide;(3-Chloro-6-methoxy-benzo[b]thiophen-2-yl)-piperidin-1-yl-methanone;(3,7-Dichloro-6-methoxy-benzo[b]thiophen-2-yl)-piperidin-1-yl-methanone;Acetic acid 1-benzoyl-decahydro-quinolin-4-yl ester;2-Bromo-N-methyl-N-phenyl-benzamide;N-Benzo[1,3]dioxol-5-yl-2,4-dichloro-benzamide;(3-Chloro-6-fluoro-benzo[b]thiophen-2-yl)-piperidin-1-yl-methanone;N-(1,2,3,5,6,7-Hexahydro-s-indacen-1-yl)-2-piperidin-1-yl-acetamide;2-[2-(1,3-Dioxo-1,3-dihydro-isoindol-2-yl)-3-phenyl-propionylamino]-3-methyl-butyricacid methyl ester; 2-(6-Oxo-6-piperidin-1-yl-hexyl)-isoindole-1,3-dione;2-[2-(1,3-Dioxo-1,3-dihydro-isoindol-2-yl)-3-phenyl-propionylamino]-3-methyl-butyricacid methyl ester; Adamantane-1-carboxylic acid(2,6-dihydroxy-pyrimidin-4-yl)-amide; Adamantane-1-carboxylic acidmethyl-phenyl-amide; 3-Chloro-benzo[b]thiophene-2-carboxylic aciddibenzylamide;N-Adamantan-1-yl-2-(3-cyano-6-methyl-4-trifluoromethyl-pyridin-2-ylsulfanyl)-acetamide;2-(3-Oxo-3-phenyl-propenyl)-isoindole-1,3-dione;N-[5-(5-Chloro-benzooxazol-2-yl)-2-methyl-phenyl]-2-methoxy-benzamide;N-[2-(2-Bromo-phenyl)-benzooxazol-5-yl]-2-methoxy-benzamide;2-(4-Chloro-phenoxy)-N-(4-chloro-3-trifluoromethyl-phenyl)-acetamide;2,2-Dimethyl-N-(5-propyl-[1,3,4]thiadiazol-2-yl)-propionamide;2-[2-(2,6-Dimethyl-morpholin-4-yl)-1-methyl-2-oxo-ethyl]-isoindole-1,3-dione;2-(2-Cyano-phenylsulfanyl)-N-(2-trifluoromethyl-phenyl)-benzamide;Azepan-1-yl-(3,6-dichloro-benzo[b]thiophen-2-yl)-methanone;Benzo[1,3]dioxol-5-yl-(4-benzyl-piperidin-1-yl)-methanone;Azepan-1-yl-(3-chloro-6-methyl-benzo[b]thiophen-2-yl)-methanone;N-(5-Hexyl-[1,3,4]thiadiazol-2-yl)-isobutyramide;(3-Chloro-phenyl)-(10,11-dihydro-dibenzo[b,f]azepin-5-yl)-methanone;(2-Chloro-phenyl)-(10,11-dihydro-dibenzo[b,f]azepin-5-yl)-methanone;2-Amino-5-(azepane-1-carbonyl)-4-methyl-thiophene-3-carboxylic acidethyl ester;Adamantan-1-yl-(4-cyclopropyl-1,4,6,7-tetrahydro-imidazo[4,5-c]pyridin-5-yl)-methanone;Adamantan-1-yl-(4-trifluoromethyl-1,4,6,7-tetrahydro-imidazo[4,5-c]pyridin-5-yl)-methanone;Adamantan-1-yl-[4-(1H-benzoimidazol-2-ylsulfanyl)-piperidin-1-yl]-methanone;Adamantan-1-yl-(1,4,6,7-tetrahydro-imidazo[4,5-c]pyridin-5-yl)-methanone;[4-(1H-Imidazol-4-yl)-piperidin-1-yl]-(4-pentyl-phenyl)-methanone;3-Cyclohexyl-1-[4-(1H-imidazol-4-yl)-piperidin-1-yl]-propan-1-one;1-(4-Propyl-piperazin-1-yl)-3-(4-trifluoromethyl-phenyl)-propan-1-one;N-(2-Hydroxy-benzyl)-3-thiophen-3-yl-N-(2-thiophen-2-yl-ethyl)-acrylamide;N-(1,3-Dimethyl-pentyl)-2-(3-fluoro-phenyl)-N-(4-hydroxy-benzyl)-acetamide;N-Cyclobutyl-2-(3-fluoro-phenyl)-N-(4-hydroxy-benzyl)-acetamide;N-Cyclobutyl-N-(4-hydroxy-benzyl)-4-trifluoromethyl-benzamide;N-(3-Hydroxy-benzyl)-2-methyl-3-nitro-N-(4-sulfamoyl-benzyl)-benzamide;N-(4-Bromo-benzyl)-N-(4-hydroxy-benzyl)-2-naphthalen-1-yl-acetamide;6-(2-Bromo-phenylsulfanyl)-hexanoic acid(3-amino-2,2-dimethyl-propyl)-amide;N-(3-Amino-2,2-dimethyl-propyl)-4-[2-(2-isopropyl-phenylsulfanyl)-ethyl]-benzamide;N-(3-Amino-2,2-dimethyl-propyl)-4-[4-(4-chloro-phenyl)-pyrimidin-2-ylsulfanylmethyl]-3-nitro-benzamide;4-(4-Bromo-phenyl)-N-(2-hydroxy-benzyl)-4-oxo-N-thiophen-2-ylmethyl-butyramide;N-[2-(2,4-Dichloro-phenyl)-ethyl]-N-(4-hydroxy-benzyl)-2-thiophen-3-yl-acetamide;N-(2-Chloro-benzyl)-N-(4-hydroxy-benzyl)-2-thiophen-2-yl-acetamide;Heptanoic acid benzyl-(4-hydroxy-benzyl)-amide;N-(4-Fluoro-benzyl)-N-(4-hydroxy-benzyl)-2-thiophen-3-yl-acetamide;4-Methyl-pentanoic acid (4-fluoro-benzyl)-(4-hydroxy-benzyl)-amide;N-Allyl-2-(4-chloro-phenyl)-N-(4-hydroxy-benzyl)-acetamide;N-Allyl-2-benzo[b]thiophen-3-yl-N-(4-hydroxy-benzyl)-acetamide;Heptanoic acid (3-ethoxy-propyl)-(4-hydroxy-benzyl)-amide; Dec-3-enoicacid (4-hydroxy-benzyl)-(4-trifluoromethyl-benzyl)-amide;6-Oxo-6-phenyl-hexanoic acid(4-hydroxy-benzyl)-(4-trifluoromethyl-benzyl)-amide;2-(3,4-Difluoro-phenyl)-N-(4-hydroxy-benzyl)-N-thiophen-2-ylmethyl-acetamide;2-Methyl-pent-4-enoic acid(3-hydroxy-benzyl)-[2-(2-methoxy-phenyl)-ethyl]-amide; Heptanoic acid(3-hydroxy-benzyl)-(4-isopropyl-benzyl)-amide;5-(2,6-Dichloro-phenylsulfanyl)-pentanoic acid(naphthalen-1-ylmethyl)-amide;N-(6,6-Dimethyl-bicyclo[3.1.1]hept-2-ylmethyl)-4-[2-(5-methyl-1H-benzoimidazol-2-ylsulfanyl)ethyl]-benzamide;N-(6,6-Dimethyl-bicyclo[3.1.1]hept-2-ylmethyl)-4-[2-(4-phenoxy-pyrimidin-2-ylsulfanyl)-ethyl]-benzamide;N-(6,6-Dimethyl-bicyclo[3.1.1]hept-2-ylmethyl)-4-[2-(4-fluoro-phenylsulfanyl)-ethyl]-benzamide;4-(2,6-Dichloro-phenylsulfanyl)-N-(6,6-dimethyl-bicyclo[3.1.1]hept-2-ylmethyl)-butyramide;5-(3-Methylsulfanyl-[1,2,4]thiadiazol-5-ylsulfanyl)-pentanoic acid(6,6-dimethyl-bicyclo[3.1.1]hept-2-ylmethyl)-amide;5-(2,6-Dichloro-phenylsulfanyl)-pentanoic acid[2-(3-trifluoromethyl-phenyl)-ethyl]-amide;4-[2-(2,6-Dichloro-phenylsulfanyl)-ethyl]-N-[2-(2-fluoro-phenyl)-ethyl]-benzamide;2-Cyclohexylamino-thiazole-4-carboxylic acid(1,2,3,4-tetrahydro-naphthalen-1-yl)-amide;2-Cyclohexylamino-thiazole-4-carboxylic acid(3-chloro-4-hydroxy-phenyl)-amide;2-Cyclohexylamino-thiazole-4-carboxylic acid(1,2-dimethyl-propyl)-amide; 2-Cyclohexylamino-thiazole-4-carboxylicacid (1-ethyl-propyl)-amide; 2-Cyclohexylamino-thiazole-4-carboxylicacid [3-(1-hydroxy-ethyl)-phenyl]-amide;2-Cyclohexylamino-thiazole-4-carboxylic acid(1-ethynyl-cyclohexyl)-amide; 2-Cyclohexylamino-thiazole-4-carboxylicacid (2-methoxy-dibenzofuran-3-yl)-amide;2-Cyclohexylamino-thiazole-4-carboxylic acid[2-(4-hydroxy-phenyl)-ethyl]-amide;2-Cyclohexylamino-thiazole-4-carboxylic acid(4-hydroxy-cyclohexyl)-amide;2-(2,6-Difluoro-benzylamino)-N-[2-(3-trifluoromethyl-phenyl)-ethyl]-acetamide;4-{4-[2-(4-Dimethylamino-phenyl)-acetyl]-piperazin-1-yl}-3-(2-phenyl-propylamino)-benzamide;2-(2-Ethyl-phenylsulfanyl)-3-[methyl-(2-pyridin-4-yl-ethyl)-amino]-N-prop-2-ynyl-propionamide;4-Methyl-cyclohexanecarboxylic acid{[2-(2-chloro-6-fluoro-benzylsulfanyl)-ethylcarbamoyl]-methyl}-prop-2-ynyl-amide;2-Benzylsulfanyl-N-{[2-(2-chloro-6-fluoro-benzylsulfanyl)-ethylcarbamoyl]-methyl}-N-(2-methoxyethyl)-acetamide;4-[2-(5-Cyclopropylmethylsulfanyl-[1,3,4]thiadiazol-2-ylsulfanyl)-ethyl]-N-(6,6-dimethyl-bicyclo[3.1.1]hept-2-ylmethyl)-benzamide;N-(6,6-Dimethyl-bicyclo[3.1.1]hept-2-ylmethyl)-2-p-tolyloxy-acetamide;Bicyclo[2.2.1]hept-5-ene-2-carboxylic acid[4-(2,5-difluoro-phenoxy)-butyl]-amide;4-Trifluoromethyl-cyclohexanecarboxylic acid[6-(2,6-difluoro-phenoxy)-hexyl]-amide;N-Cyclopropyl-3-methoxy-N-(2-piperidin-4-yl-ethyl)-5-(pyridine-2-carbonyl)-benzamide;3-Methoxy-N-(2-methoxy-ethyl)-N-(2-piperidin-4-yl-ethyl)-5-(pyridine-2-carbonyl)-benzamide;3-Methoxy-N-(2-piperidin-4-yl-ethyl)-5-(pyridine-2-carbonyl)-N-(tetrahydro-furan-2-ylmethyl)benzamide;3-Methoxy-N-(2-oxo-azepan-3-yl)-N-(2-piperidin-4-yl-ethyl)-5-(pyridine-2-carbonyl)-benzamide;3-Methoxy-N-[3-(2-oxo-pyrrolidin-1-yl)-propyl]-N-(2-piperidin-4-yl-ethyl)-5-(pyridine-2-carbonyl)benzamide;3-Methoxy-N-methyl-N-(2-piperidin-4-yl-ethyl)-5-(pyridine-2-carbonyl)-benzamide;[2-({Cyclopropyl-[3-methoxy-5-(pyridine-2-carbonyl)-benzoyl]-amino}-methyl)-phenoxy]-aceticacid;(2-{[[3-Methoxy-5-(pyridine-2-carbonyl)-benzoyl]-(3-methyl-butyl)-amino]-methyl}-phenoxy)aceticacid;[2-({Cyclopentyl-[3-methoxy-5-(pyridine-2-carbonyl)-benzoyl]-amino}-methyl)-phenoxy]-aceticacid;[2-({(2-Methoxy-ethyl)-[3-methoxy-5-(pyridine-2-carbonyl)-benzoyl]-amino}-methyl)-phenoxy]-aceticacid;[2-({Carbamoylmethyl-[3-methoxy-5-(pyridine-2-carbonyl)-benzoyl]-amino}-methyl)-phenoxy]-aceticacid;[2-({[3-Methoxy-5-(pyridine-2-carbonyl)-benzoyl]-pyridin-4-yl-amino}-methyl)-phenoxy]-aceticacid;[2-({Cyclopropylmethyl-[3-methoxy-5-(pyridine-2-carbonyl)-benzoyl]-amino}-methyl)-phenoxy]-aceticacid;[2-({[3-Methoxy-5-(pyridine-2-carbonyl)-benzoyl]-methyl-amino}-methyl)-phenoxy]-aceticacid;[4-(4-Hydroxy-benzyl)-piperazin-1-yl]-[3-methoxy-5-(pyridine-2-carbonyl)-phenyl]-methanone;{Carbamoylmethyl-[3-methoxy-5-(pyridine-2-carbonyl)-benzoyl]-amino}-aceticacid;{(3-Imidazol-1-yl-propyl)-[3-methoxy-5-(pyridine-2-carbonyl)-benzoyl]-amino}-aceticacid;{[3-Methoxy-5-(pyridine-2-carbonyl)-benzoyl]-pyridin-4-yl-amino}-aceticacid;[[3-Methoxy-5-(pyridine-2-carbonyl)-benzoyl]-(2-oxo-azepan-3-yl)-amino]-aceticacid;3-Methoxy-N-(2-methoxy-ethyl)-N-piperidin-3-ylmethyl-5-(pyridine-2-carbonyl)-benzamide;4-[3-Methoxy-5-(pyridine-2-carbonyl)-benzoylamino]-piperidine-1-carboxylicacid ethyl ester;3-Methoxy-N-[3-(2-oxo-pyrrolidin-1-yl)-propyl]-5-(pyridine-2-carbonyl)-benzamide;3-({Carbamoylmethyl-[3-methoxy-5-(pyridine-2-carbonyl)-benzoyl]-amino}-methyl)-benzoicacid;3-({(3-Imidazol-1-yl-propyl)-[3-methoxy-5-(pyridine-2-carbonyl)-benzoyl]-amino}-methyl)-benzoicacid;4-Amino-N-(3-hydroxy-benzyl)-N-indan-2-yl-2-propionylamino-butyramide;5-Amino-2-propionylamino-pentanoic acid(3-hydroxy-benzyl)-indan-2-yl-amide;N-Ethyl-2-hexylamino-N-(4-hydroxy-benzyl)-acetamide;2-Hexylamino-N-(4-hydroxy-benzyl)-N-methyl-acetamide;1-[1-(6-Phenyl-hexanoyl)-piperidin-4-yl]-1,3-dihydro-benzoimidazol-2-one;1-[1-(3-Cyclohexyl-propionyl)-piperidin-4-yl]-1,3-dihydro-benzoimidazol-2-one;N-(2-Hydroxy-benzyl)-N-isobutyl-benzamide;N-(2-Hydroxy-benzyl)-2-(4-hydroxy-phenyl)-N-isobutyl-acetamide;N-(2-Hydroxy-benzyl)-N-(3-methyl-butyl)-benzamide;N-(4-Hydroxy-benzyl)-N-isobutyl-benzamide;4-Hydroxy-N-(4-hydroxy-benzyl)-N-isobutyl-benzamide;N-(4-Hydroxy-benzyl)-2-(4-hydroxy-phenyl)-N-isobutyl-acetamide;N-(4-Hydroxy-benzyl)-N-(3-methyl-butyl)-benzamide;N-(2-Ethoxy-ethyl)-4-hydroxy-N-(4-hydroxy-benzyl)-benzamide;N-(4-Hydroxy-benzyl)-N-(3-isopropoxy-propyl)-benzamide;N-(3-Hydroxy-benzyl)-N-(4-methyl-pentyl)-benzamide;N-(3-Hydroxy-benzyl)-2-(4-hydroxy-phenyl)-N-(4-methyl-pentyl)-acetamide;N-(3-Hydroxy-benzyl)-N-(3-isopropoxy-propyl)-benzamide;N-(2-Hydroxy-benzyl)-N-(3-methyl-butyl)-4-propyl-benzamide;N-(4-Hydroxy-benzyl)-N-(6-hydroxy-hexyl)-4-propyl-benzamide;N-(4-Hydroxy-benzyl)-N-(3-methyl-butyl)-4-propyl-benzamide; andN-[2-(4-Fluoro-benzylamino)-thiazol-4-ylmethyl]-N-phenethyl-butyramide;or a salt thereof with a pharmaceutically acceptable acid or base, oroptical isomer or mixture of optical isomers, racemic mixture, ortautomeric forms thereof.
 16. A pharmaceutical composition comprising atherapeutically effective amount of a compound according to claim 3,together with one or more pharmaceutically acceptable carriers orexcipients.
 17. The pharmaceutical composition according to claim 16,wherein the pharmaceutical composition is for oral, nasal, buccal,transdermal, pulmonal or parenteral administration.
 18. Thepharmaceutical composition according to claim 16, wherein thepharmaceutical composition is in unit dosage form, comprising from about0.05 mg to about 2000 mg/day, from about 0.1 mg to about 1000 mg, orfrom about 0.5 mg to about 500 mg per day of the compound.
 19. A methodfor the treatment, prevention and/or prophylaxis of conditions,disorders or diseases wherein a modulation or an inhibition of theactivity of 11βHSD1 is beneficial, the method comprising administeringto a subject in need thereof an effective amount of a compound accordingto claim
 3. 20. The method according to claim 19, wherein the treatment,prevention and/or prophylaxis is of any conditions, disorders anddiseases that are influenced by intracellular glucocorticoid levels. 21.The method according to claim 19 or 20, wherein the condition, disorderor disease is the metabolic syndrome, insulin resistance, dyslipidemia,hypertension and obesity.
 22. The method according to claim 19 or 20,wherein the condition, disorder or disease is type 2 diabetes, impairedglucose tolerance (IGT), impaired fasting glucose (IFG).
 23. The methodaccording to claim 19 or 20, for the delaying or prevention of theprogression from IGT to type 2 diabetes.
 24. The method according toclaim 19 or 20, for the delaying or prevention of the progression of themetabolic syndrome into type 2 diabetes.
 25. The method according toclaim 19 or 20, wherein the condition, disorder or disease is diabeticlate complications including cardiovascular diseases; arteriosclerosis;atherosclerosis.
 26. The method according to claim 19 or 20, wherein thecondition, disorder or disease is neurodegenerative and psychiatricdisorders.
 27. The method according to claim 19 or 20, for thetreatment, prevention and/or prophylaxis of adverse effects ofglucocorticoid receptor agonist treatment or therapy.
 28. A compound offormula (II)

wherein R¹ is C₃-C₁₀cycloalkyl or C₃-C₁₀hetcycloalkyl, wherein thecycloalkyl and hetcycloalkyl groups independently are optionallysubstituted with one or more of R⁴; R² is hydrogen, C₁-C₈alkyl,arylC₁-C₆alkyl, wherein the alkyl and aryl groups independently areoptionally substituted with one or more of R⁵; or R¹ and R² togetherwith the nitrogen to which they are attached, are forming a saturated orpartially saturated cyclic, bicyclic or tricyclic ring system containingfrom 4 to 10 carbon atoms and from 0 to 2 additional heteroatomsselected from nitrogen, oxygen or sulphur, the ring system optionallybeing substituted with at least one of C₁-C₈alkyl, aryl, hetaryl,arylC₁-C₆alkyl, hetarylC₁-C₆alkyl, hydroxy, oxo, cyano, C₁-C₆alkyloxy,arylC₁-C₆alkyloxy, hetarylC₁-C₆alkyloxy, C₁-C₆alkyloxyC₁-C₆alkyl,C₁-C₆alkylcarbonyl, arylcarbonyl, hetarylcarbonyl,arylC₁-C₆alkylcarbonyl, hetarylC₁-C₆alkylcarbonyl, C₁-C₆alkylcarboxy,arylcarboxy or arylC₁-C₆alkylcarboxy wherein the alkyl and aryl groupsindependently are optionally substituted with one or more of R¹⁴; R³ isC₃-C₁₀cycloalkyl, C₃-C₁₀hetcycloalkyl, aryl or hetaryl, wherein thealkyl, cycloalkyl, hetcycloalkyl, aryl and hetaryl groups independentlyare optionally substituted with one or more of R⁷; R⁴ and R⁵independently are hydrogen, hydroxy, oxo, cyano, halo, methylendioxo,NR⁸R⁹, C₁-C₈alkyl, C₁-C₆alkyloxy, trihalomethyl, trihalomethyloxy,C₃-C₁₀cycloalkyl, C₃-C₁₀hetcycloalkyl, C₃-C₁₀cycloalkenyl, aryl,hetaryl, hetarylSO_(n), arylC₁-C₆alkyloxy, hetarylC₁-C₆alkyloxy,C₁-C₆alkyl-R⁶—C₁-C₆alkyl, arylC₁-C₆alkyl-R⁶—C₁-C₆alkyl,C₁-C₆alkylcarbonyl, arylcarbonyl, arylC₁-C₆alkylcarbonyl,hetarylcarbonyl, hetarylC₁-C₆alkylcarbonyl, C₁-C₆alkylSO_(n),C₁-C₆alkylcarboxy, arylcarboxy, hetarylcarboxy, arylC₁-C₆alkylcarboxy orhetarylC₁-C₆alkylcarboxy wherein the alkyl, cycloalkyl, hetcycloalkyl,aryl and hetaryl groups independently are optionally substituted withone or more of R¹⁵; R⁶ is oxygen, sulphur, SO_(n) or NR¹⁶; R⁷ ishydrogen, halo, hydroxy, cyano, nitro, COOR¹⁷, C₁-C₈alkyl,C₃-C₁₀cycloalkyl, C₃-C₁₀hetcycloalkyl, methylendioxo, trihalomethyl,trihalomethyloxy, aryl, arylC₁-C₆alkyl, C₁-C₆alkyloxy,C₁-C₆alkyloxyC₁-C₆alkyl, aryloxy, arylC₁-C₆alkyloxy, aryloxyC₁-C₆alkyl,arylC₁-C₆alkyloxyC₁-C₆alkyl, hetaryl, hetarylC₁-C₆alkyl, hetaryloxy,hetarylC₁-C₆alkyloxy, hetaryloxyC₁-C₆alkyl,hetarylC₁-C₆alkyl-oxyC₁-C₆alkyl, NR⁸R⁹, SO_(m)NR⁸R⁹,NR⁴R⁵carbonylC₁-C₆alkyl, arylthio, hetarylthio, R¹⁸carbonylNR⁸,arylSO_(n), hetarylSO_(n), R¹⁹SO_(m)NR⁸, arylthioC₁-C₆alkyl,hetarylthioC₁-C₆alkyl or arylC₁-C₆alkylR⁶C₁-C₆alkyl; wherein the aryland hetaryl groups independently are optionally substituted with one ormore R¹⁰; R⁸ and R⁹ independently are hydrogen, C₁-C₈alkyl, aryl,hetaryl, C₁-C₆alkylSO_(m), arylSO_(m), arylC₁-C₆alkylSO_(m),arylC₁-C₆alkyl or hetarylC₁-C₆alkyl wherein the alkyl, aryl and hetarylgroups independently are optionally substituted with one or more of R¹¹;or R⁸ and R⁹ together with the nitrogen to which they are attached, areforming a saturated or partially saturated cyclic, bicyclic or tricyclicring system containing from 4 to 10 carbon atoms and from 0 to 2additional heteroatoms selected from nitrogen, oxygen or sulfur, thering system optionally being substituted with at least one halo, cyano,C₁-C₈alkyl, aryl, hetaryl, arylC₁-C₆alkyl, hetarylC₁-C₆alkyl, hydroxy,oxo, C₁-C₆alkyloxy, arylC₁-C₆alkyloxy, hetarylC₁-C₆alkyloxy,C₁-C₆alkyloxyC₁-C₆alkyl, C₁-C₆alkylcarbonyl, arylcarbonyl,hetarylcarbonyl, arylC₁-C₆alkylcarbonyl, hetarylC₁-C₆alkylcarbonyl,C₁-C₆alkylcarboxy, arylcarboxy, hetarylcarboxy, arylC₁-C₆alkylcarboxy orhetarylC₁-C₆alkylcarboxy; R¹⁰ and R¹¹ independently are hydrogen,hydroxy, oxo, halo, cyano, nitro, C₁-C₈alkyl, C₁-C₆alkyl-oxy, NR¹²R¹³,methylendioxo, trihalomethyl or trihalomethyloxy; R¹² and R¹³independently are hydrogen, C₁-C₈alkyl or arylC₁-C₆alkyl; R¹⁴ ishydrogen, halo, hydroxy, oxo, nitro, cyano, C₁-C₈alkyl, C₁-C₆alkyloxy oraryloxy; R¹⁵ is hydrogen, halo, hydroxy, oxo, nitro, cyano, CONR⁸R⁹ orCOOR¹⁷; R¹⁶ is hydrogen, C₁-C₈alkyl, C₃-C₁₀cycloalkyl,C₃-C₁₀hetcycloalkyl, aryl, arylC₁-C₆alkyl, hetaryl, hetarylC₁-C₆alkyl,alkylcarbonyl, arylcarbonyl, arylC₁-C₆alkylcarbonyl, aryloxyC₁-C₆alkyl,hetaryloxyC₁-C₆alkyl, arylthioC₁-C₆alkyl or hetarylthioC₁-C₆alkyl;wherein the alkyl, cycloalkyl, hetcycloalkyl, aryl and hetaryl groupsindependently are optionally substituted with one or more of R¹⁰; R¹⁷ ishydrogen, C₁-C₈alkyl, aryl or arylC₁-C₆alkyl; R¹⁸ is C₁-C₆alkyl,C₂-C₆alkenyl, aryl, arylC₁-C₆alkyl, hetaryl, hetarylC₁-C₆alkyl,C₃-C₁₀cycloalkyl, C₃-C₁₀hetcycloalkyl, C₁-C₆alkyloxy, aryloxy,arylC₁-C₆alkyloxy, arylC₁-C₆alkyloxyC₁-C₆alkyl,hetarylC₁-C₆alkyloxyC₁-C₆alkyl, hetaryloxy, hetarylC₁-C₆alkyloxy orR⁸R⁹NC₁-C₆alkyl wherein the alkyl, alkenyl, cycloalkyl, hetcycloalkyl,aryl and hetaryl groups are optionally substituted with R¹⁵; R¹⁹ isC₁-C₆alkyl, C₃-C₁₀cycloalkyl, C₃-C₁₀hetcycloalkyl, aryl, arylC₁-C₆alkyl,hetaryl, hetarylC₁-C₆alkyl; m is 1 or 2; n is 0, 1 or 2; or a saltthereof with a pharmaceutically acceptable acid or base, or opticalisomer or mixture of optical isomers, racemic mixture, or tautomericforms thereof.
 29. A compound according to claim 28, wherein R¹ isC₃-C₁₀cycloalkyl or C₃-C₁₀hetcycloalkyl, wherein the cycloalkyl andhetcycloalkyl groups independently are optionally substituted with oneor more of R⁴.
 30. A compound according to claim 28, wherein R² ishydrogen or C₁-C₈alkyl.
 31. A compound according to claim 28, wherein R¹and R² together with the nitrogen to which they are attached, areforming a saturated or partially saturated cyclic, bicyclic or tricyclicring system containing from 4 to 10 carbon atoms and from 0 to 2additional heteroatoms selected from nitrogen, oxygen or sulphur, thering system optionally being substituted with at least one ofC₁-C₈alkyl, aryl, hetaryl, arylC₁-C₆alkyl, hetarylC₁-C₆alkyl, hydroxy,oxo, cyano, C₁-C₆alkyloxy, arylC₁-C₆alkyloxy, hetarylC₁-C₆alkyloxy,C₁-C₆alkyloxyC₁-C₆alkyl, C₁-C₆alkylcarbonyl, arylcarbonyl,hetarylcarbonyl, arylC₁-C₆alkylcarbonyl, hetarylC₁-C₆alkylcarbonyl,C₁-C₆alkylcarboxy, arylcarboxy or arylC₁-C₆alkylcarboxy wherein thealkyl and aryl groups independently are optionally substituted with oneor more of R¹⁴.
 32. A compound according to claim 28, wherein R³ is arylor hetaryl, wherein the aryl and hetaryl groups independently areoptionally substituted with one or more of R⁷.
 33. A compound accordingto claim 28, wherein R⁴ and R⁵ independently are hydrogen, hydroxy, oxo,halo, C₁-C₈alkyl, wherein the alkyl group is optionally substituted withone or more of R¹⁵.
 34. A compound according to claim 28, wherein R⁷ ishydrogen, halo, hydroxy, cyano, C₁-C₈alkyl, C₃-C₁₀cycloalkyl,C₃-C₁₀hetcycloalkyl, trihalomethyl, aryl, arylC₁-C₆alkyl, C₁-C₆alkyloxy,C₁-C₆alkyloxyC₁-C₆alkyl, aryloxy, arylC₁-C₆alkyloxy, aryloxyC₁-C₆alkyl,arylC₁-C₆alkyloxyC₁-C₆alkyl, hetaryl, hetarylC₁-C₆alkyl, hetaryloxy,hetarylC₁-C₆alkyloxy, hetaryloxyC₁-C₆alkyl,hetarylC₁-C₆alkyl-oxyC₁-C₆alkyl, NR⁸R⁹, R¹⁸carbonylNR⁸, R¹⁹SO_(m)NR⁸;wherein the aryl and hetaryl groups independently are optionallysubstituted with one or more R¹⁰.
 35. A compound according to claim 28,wherein R⁸ and R⁹ together with the nitrogen to which they are attached,are forming a saturated or partially saturated cyclic, bicyclic ortricyclic ring system containing from 4 to 10 carbon atoms and from 0 to2 additional heteroatoms selected from nitrogen, oxygen or sulfur, thering system optionally being substituted with at least one halo, cyano,C₁-C₈alkyl, aryl, hetaryl, arylC₁-C₆alkyl, hetarylC₁-C₆alkyl, hydroxy,oxo, C₁-C₆alkyloxy, arylC₁-C₆alkyloxy, hetarylC₁-C₆alkyloxy,C₁-C₆alkyloxyC₁-C₆alkyl, C₁-C₆alkylcarbonyl, arylcarbonyl,hetarylcarbonyl, arylC₁-C₆alkylcarbonyl, hetarylC₁-C₆alkylcarbonyl,C₁-C₆alkylcarboxy, arylcarboxy, hetarylcarboxy, arylC₁-C₆alkylcarboxy orhetarylC₁-C₆alkylcarboxy.
 36. A compound according to claim 28, whereinR¹⁵ is CONR⁸R⁹.
 37. A compound according to claim 28, wherein R¹⁸ isC₁-C₆alkyl.
 38. A compound according to claim 28, which is:(4-Tetrazol-1-yl-phenyl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone;N-Cyclohexyl-N-methyl-2-phenoxymethyl-benzamide;4-Amino-N-cyclohexyl-N-methyl-benzamide;N-Cycloheptyl-N-methyl-2-phenoxymethyl-benzamide;N-Cyclohexyl-N-methyl-benzamide;2-Chloro-N-cyclohexyl-6-fluoro-N-methyl-benzamide;N-Cyclohexyl-N-methyl-4-trifluoromethoxy-benzamide; N-Cyclohexyl-2,3,N-trimethyl-benzamide; 3,5-Dichloro-N-cyclohexyl-N-methyl-benzamide;N-Cyclohexyl-N-methyl-2-phenoxy-benzamide;2,4-Bis-benzyloxy-N-cyclohexyl-N-methyl-benzamide;2-Benzyloxy-N-cyclohexyl-N-methyl-benzamide;N-Cyclohexyl-N-methyl-4-phenoxy-benzamide;4-Benzyloxy-N-cyclohexyl-N-methyl-benzamide;N-Cyclohexyl-N-methyl-4-phenoxymethyl-benzamide;2-Chloro-N-cyclohexyl-N-ethyl-4-nitro-benzamide;4-Chloro-N-cyclohexyl-N-ethyl-3-nitro-benzamide;6-Fluoro-4H-benzo[1,3]dioxine-8-carboxylic acid cyclohexyl-methyl-amide;Azepan-1-yl-(2-chloro-phenyl)-methanone;Azepan-1-yl-(3-chloro-phenyl)-methanone; Azepan-1-yl-phenyl-methanone;2-(Biphenyl-4-yloxy)-N-cyclohexyl-N-methyl-benzamide;N-Cyclohexyl-2-(3,5-dimethoxy-phenoxy)-N-methyl-benzamide;N-Cyclohexyl-2-(2,3-dimethoxy-phenoxy)-N-methyl-benzamide;2,4-Dichloro-N-(3,3-dimethyl-1,5-dioxa-spiro[5.5]undec-9-yl)-N-methyl-benzamide;2,4-Dichloro-N-methyl-N-(4-oxo-cyclohexyl)-benzamide;N-Cyclohexyl-2-hydroxy-N-methyl-benzamide;N-Cyclohexyl-3-methoxy-N-methyl-benzamide;Benzo[1,3]dioxole-5-carboxylic acid cyclohexyl-methyl-amide;3-Benzyloxy-N-cyclohexyl-N-methyl-benzamide;N-Cyclohexyl-3-hydroxy-N-methyl-benzamide;[4-(Morpholine-4-sulfonyl)-phenyl]-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone;N-Benzyl-3-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]octane-6-carbonyl)-benzenesulfonamide;[4-Fluoro-3-(morpholine-4-sulfonyl)-phenyl]-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone;Thiophene-2-sulfonic acid[4-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]octane-6-carbonyl)-phenyl]-amide;N-Phenyl-4-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]octane-6-carbonyl)-benzenesulfonamide;(4-Phenoxy-phenyl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone;N-(2,4-Dimethyl-phenyl)-3-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]octane-6-carbonyl)benzenesulfonamide;(2-Phenoxymethyl-phenyl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone;4-(3-Aza-bicyclo[3.2.2]nonane-3-carbonyl)-N,N-dipropyl-benzenesulfonamide;2-Bromo-N-cyclohexyl-N-methyl-benzamide;N-[4-(1,3,3-Trimethyl-6-aza-bicyclo[3.2.1]octane-6-carbonyl)-phenyl]-acetamide;(4-Dimethylamino-phenyl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone;(4-Pyrrol-1-yl-phenyl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone;(4-Imidazol-1-yl-phenyl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone;(4-Amino-2-methoxy-phenyl)-(trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone;(4-Methanesulfonyl-phenyl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone;(3-Methanesulfonyl-phenyl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone;(4-Benzenesulfonyl-phenyl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone;Azepan-1-yl-[4-(3,4-dihydro-1H-isoquinolin-2-ylmethyl)-phenyl]-methanone;Azepan-1-yl-(4-morpholin-4-ylmethyl-phenyl)-methanone;[4-(3-Trifluoromethyl-pyrazol-1-yl)-phenyl]-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone;(4-[1,2,4]Triazol-1-yl-phenyl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone;(4-Pyrazol-1-yl-phenyl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone;2-Benzyloxymethyl-N-cyclohexyl-N-methyl-benzamide;N-Cyclohexyl-N-methyl-4-(3-methyl-5-oxo-4,5-dihydro-pyrazol-1-yl)-benzamide;5-Methyl-2-[4-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]octane-6-carbonyl)-phenyl]-2,4-dihydropyrazol-3-one;(9H-Carbazol-3-yl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone;[4-(3,5-Dimethyl-pyrazol-1-yl)-phenyl]-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone;Phenyl-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone;Azepan-1-yl-(2-bromo-phenyl)-methanone;(3-Aza-bicyclo[3.2.2]non-3-yl)-(2-bromo-phenyl)-methanone;(4-Benzyl-piperidin-1-yl)-quinolin-2-yl-methanone;(2-Methyl-piperidin-1-yl)-quinolin-2-yl-methanone;(3-Aza-bicyclo[3.2.2]non-3-yl)-quinolin-2-yl-methanone;Quinoline-2-carboxylic acid cyclohexyl-methyl-amide;Quinolin-2-yl-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone;1-[4-(1,3,3-Trimethyl-6-aza-bicyclo[3.2.1]octane-6-carbonyl)-phenyl]-pyrrolidine-2,5-dione;Pyridin-3-yl-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone;Pyridin-4-yl-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone;Pyridin-2-yl-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone;(6-Pyrazol-1-yl-pyridin-3-yl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone;4-(1,3,3-Trimethyl-6-aza-bicyclo[3.2.1]octane-6-carbonyl)-benzoic acid;Imidazo[2,1-b]thiazol-6-yl-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone;8-(4-Dimethylamino-benzoyl)-8-aza-bicyclo[3.2.1]octan-3-one;(4-Dimethylamino-phenyl)-(3-hydroxy-8-aza-bicyclo[3.2.1]oct-8-yl)-methanone;(4-Dimethylamino-phenyl)-(3-hydroxy-3-methyl-8-aza-bicyclo[3.2.1]oct-8-yl)-methanone;and Trifluoro-acetic acid8-(4-dimethylamino-benzoyl)-8-aza-bicyclo[3.2.1]oct-3-yl ester; or asalt thereof with a pharmaceutically acceptable acid or base, or opticalisomer or mixture of optical isomers, racemic mixture, or tautomericforms thereof.
 39. A compound of formula (III):

wherein R¹ is aryl, arylC₁-C₆alkyl, hetaryl or hetarylC₁-C₆alkyloptionally substituted with one or more of R⁶ independently; R² is halo,C₁-C₆alkyl, C₂-C₆alkenyl, C₂-C₆alkynyl, C₃-C₁₀cycloalkyl,C₃-C₁₀cycloalkylC₁-C₆alkyl, trihalomethyl, aryl, arylC₁-C₆alkyl,C₁-C₆alkyloxyC₁-C₆alkyl, arylC₁-C₆alkyloxyC₁-C₆alkyl,C₁-C₆-alkylNR⁵C₁-C₆alkyl, arylC₁-C₆alkylNR⁵C₁-C₆alkyl, hetaryl orhetarylC₁-C₆alkyl wherein the alkyl, alkenyl, alkynyl, cycloalkyl andaryl groups independently are optionally substituted with one or moreR⁷; R³ is C₁-C₆alkyl optionally substituted with one or more of R⁸; R⁴is C₆-C₁₀cycloalkyl, C₆-C₁₀hetcycloalkyl, C₆-C₁₀cycloalkylC₁-C₆alkyl orC₆-C₁₀hetcycloalkylC₁-C₆alkyl wherein the alkyl, cycloalkyl andhetcycloalkyl groups independently are optionally substituted with oneor more of R⁸; or R³ and R⁴ together with the nitrogen to which they areattached, are forming a saturated or partially saturated bicyclic/bridgering system containing from 7 to 12 carbon atoms and from 0 to 2additional heteroatoms selected from nitrogen, oxygen or sulphur, thering system optionally being substituted with at least one ofC₁-C₆alkyl, aryl, hetaryl, arylC₁-C₆alkyl, hetarylC₁-C₆alkyl, hydroxy,oxo, C₁-C₆alkyloxy, arylC₁-C₆alkyloxy or hetarylC₁-C₆alkyloxy, whereinthe alkyl and aryl groups independently are optionally substituted withone or more of R⁹; R⁵ is C₁-C₆alkyl, C₂-C₆alkenyl, C₂-C₆alkynyl,C₃-C₁₀cycloalkyl, C₃-C₁₀hetcycloalkyl, C₃-C₁₀-cycloalkylC₁-C₆alkyl,C₃-C₁₀hetcycloalkylC₁-C₆alkyl, aryl, hetaryl, arylC₁-C₆alkyl orhetarylC₁-C₆alkyl wherein the alkyl, alkenyl, alkynyl, aryl, hetaryl,cycloalkyl and hetcycloalkyl groups independently are optionallysubstituted with one or more of R⁹; R⁶ and R⁷ independently arehydrogen, hydroxy, oxo, halo, nitro, cyano, C₁-C₆alkyl, C₁-C₆-alkyloxy,trihalomethyl, trihalomethoxy, NR¹⁰R¹¹, arylC₁-C₆alkyloxy,hetarylC₁-C₆alkyloxy, C₁-C₆-alkylcarbonyl, arylcarbonyl,hetarylcarbonyl, arylC₁-C₆alkylcarbonyl, C₁-C₆alkyloxycarbonyl,aryloxycarbonyl, arylC₁-C₆alkyloxycarbonyl, C₁-C₆alkylcarboxy,arylcarboxy or arylC₁-C₆alkylcarboxy; R⁸ and R⁹ independently arehydrogen, C₁-C₆alkyl, aryl, hetaryl, arylC₁-C₆alkyl, hetarylC₁-C₆-alkyl,hydroxy, oxo, cyano, NR¹⁰R¹¹, C₁-C₆alkyloxy, aryloxy, arylC₁-C₆alkyloxy,hetaryloxy, hetarylC₁-C₆alkyloxy, C₁-C₆alkyloxyC₁-C₆alkyl,C₁-C₆alkylcarbonyl, arylcarbonyl, hetarylcarbonyl,arylC₁-C₆alkylcarbonyl, hetarylC₁-C₆alkylcarbonyl, C₁-C₆alkylcarboxy,arylcarboxy or arylC₁-C₆alkylcarboxy; R¹⁰ and R¹¹ independently arehydrogen, C₁-C₈alkyl, aryl, hetaryl, arylC₁-C₆alkyl, C₃-C₁₀-cycloalkyl,C₃-C₁₀hetcycloalkyl, C₃-C₁₀cycloalkylC₁-C₆alkyl, C₁-C₆alkylcarbonyl,C₁-C₆alkylcarboxyC₁-C₆alkyl; or R¹⁰ and R¹¹ together with the nitrogento which they are attached, are forming a saturated or partiallysaturated cyclic, bicyclic or tricyclic ring system containing from 4 to10 carbon atoms and from 0 to 2 additional heteroatoms selected fromnitrogen, oxygen or sulphur, the ring system optionally beingsubstituted with at least one of C₁-C₈alkyl, aryl, hetaryl,arylC₁-C₆alkyl, hetarylC₁-C₆alkyl, hydroxy, oxo, cyano, C₁-C₆alkyloxy,arylC₁-C₆alkyloxy, hetarylC₁-C₆alkyloxy, C₁-C₆alkyloxyC₁-C₆alkyl,C₁-C₆alkylcarbonyl, arylcarbonyl, hetarylcarbonyl,arylC₁-C₆alkylcarbonyl, hetarylC₁-C₆alkylcarbonyl, C₁-C₆alkylcarboxy,arylcarboxy or arylC₁₋₆-alkylcarboxy; or a salt thereof with apharmaceutically acceptable acid or base, or optical isomer or mixtureof optical isomers, racemic mixture, or tautomeric forms thereof.
 40. Acompound according to claim 39, wherein R¹ is aryl or hetaryl optionallysubstituted with one or more R⁶ independently; R² is halo, C₁-C₆alkyl,C₂-C₆alkenyl, C₂-C₆alkynyl, C₃-C₁₀cycloalkyl,C₃-C₁₀cycloalkylC₁-C₆alkyl, aryl, arylC₁-C₆alkyl,C₁-C₆alkyloxyC₁-C₆alkyl, arylC₁-C₆alkyloxyC₁-C₆alkyl,C₁-C₆alkylNR⁵C₁-C₆alkyl, arylC₁-C₆alkylNR⁵C₁-C₆alkyl, hetaryl orhetarylC₁-C₆alkyl wherein the alkyl, alkenyl, alkynyl, cycloalkyl andaryl groups independently are optionally substituted with one or moreR⁷; R³ is C₁-C₆alkyl optionally substituted with one or more of R⁸; R⁴is C₆-C₁₀cycloalkyl, C₆-C₁₀hetcycloalkyl, C₆-C₁₀cycloalkylC₁-C₆alkyl orC₆-C₁₀hetcycloalkylC₁-C₆alkyl wherein the alkyl, cycloalkyl andhetcycloalkyl groups independently are optionally substituted with oneor more of R⁸; R⁵ is C₁-C₆alkyl, C₂-C₆alkenyl, C₂-C₆alkynyl,C₃-C₁₀cycloalkyl, C₃-C₁₀hetcycloalkyl, C₃-C₁₀-cycloalkylC₁-C₆alkyl,C₃-C₁₀hetcycloalkylC₁-C₆alkyl, aryl, hetaryl, arylC₁-C₆alkyl orhetarylC₁-C₆alkyl wherein the alkyl, alkenyl, alkynyl, aryl, hetaryl,cycloalkyl and hetcycloalkyl groups independently are optionallysubstituted with one or more of R⁹; R⁶ and R⁷ independently arehydrogen, hydroxy, oxo, halo, nitro, cyano, C₁-C₆alkyl, C₁-C₆-alkyloxy,trihalomethyl, trihalomethoxy, NR¹⁰R¹¹, arylC₁-C₆alkyloxy,hetarylC₁-C₆alkyloxy, C₁-C₆-alkylcarbonyl, arylcarbonyl,hetarylcarbonyl, arylC₁-C₆alkylcarbonyl, C₁-C₆alkyloxycarbonyl,aryloxycarbonyl, arylC₁-C₆alkyloxycarbonyl, C₁-C₆alkylcarboxy,arylcarboxy or arylC₁-C₆alkylcarboxy; R⁸ and R⁹ independently arehydrogen, C₁-C₆alkyl, aryl, hetaryl, arylC₁-C₆alkyl, hetarylC₁-C₆-alkyl,hydroxy, oxo, cyano, NR¹⁰R¹¹, C₁-C₆alkyloxy, aryloxy, arylC₁-C₆alkyloxy,hetaryloxy, hetarylC₁-C₆alkyloxy, C₁-C₆alkyloxyC₁-C₆alkyl,C₁-C₆alkyl-carbonyl, arylcarbonyl, hetarylcarbonyl,arylC₁-C₆alkylcarbonyl, hetarylC₁-C₆alkyl-carbonyl, C₁-C₆alkylcarboxy,arylcarboxy or arylC₁-C₆alkylcarboxy; R¹⁰ and R¹¹ independently arehydrogen, C₁-C₈alkyl, aryl, hetaryl, arylC₁-C₆alkyl, C₃-C₁₀-cycloalkyl,C₃-C₁₀hetcycloalkyl, C₃-C₁₀cycloalkylC₁-C₆alkyl,C₁-C₆alkylcarboxyC₁-C₆alkyl; or R¹⁰ and R¹¹ together with the nitrogento which they are attached, are forming a saturated or partiallysaturated cyclic, bicyclic or tricyclic ring system containing from 4 to10 carbon atoms and from 0 to 2 additional heteroatoms selected fromnitrogen, oxygen or sulphur, the ring system optionally beingsubstituted with at least one of C₁-C₈alkyl, aryl, hetaryl,arylC₁-C₆alkyl, hetarylC₁-C₆alkyl, hydroxy, oxo, cyano, C₁-C₆alkyloxy,arylC₁-C₆alkyloxy, hetaryl C₁-C₆alkyloxy, C₁-C₆alkyloxyC₁-C₆alkyl,C₁-C₆alkylcarbonyl, arylcarbonyl, hetarylcarbonyl,arylC₁-C₆alkylcarbonyl, hetarylC₁-C₆alkylcarbonyl, C₁-C₆alkylcarboxy,arylcarboxy or arylC₁₋₆-alkylcarboxy; or a salt thereof with apharmaceutically acceptable acid or base, or optical isomer or mixtureof optical isomers, racemic mixture, a prodrug thereof, or tautomericforms thereof.
 41. A compound according to claim 39, wherein R¹ is aryl,arylC₁-C₆alkyl or hetaryl optionally substituted with one or more of R⁶.42. A compound according to claim 39, wherein R² is C₁-C₆alkyl,C₃-C₁₀cycloalkyl, C₃-C₁₀cycloalkylC₁-C₆alkyl, trihalomethyl,arylC₁-C₆alkyl, or hetarylC₁-C₆alkyl wherein the alkyl, cycloalkyl andaryl groups independently are optionally substituted with one or moreR⁷.
 43. A compound according to claim 39, wherein R³ is C₁-C₆alkyloptionally substituted with one or more of R⁸.
 44. A compound accordingto claim 39, wherein R⁴ is C₆-C₁₀cycloalkyl, or C₆-C₁₀hetcycloalkyl,wherein the cycloalkyl and hetcycloalkyl groups independently areoptionally substituted with one or more of R³.
 45. A compound accordingto claim 39, wherein R⁶ and R⁷ independently are hydrogen, hydroxy, oxo,halo, cyano, C₁-C₆alkyl, C₁-C₆alkyloxy, trihalomethyl, NR¹⁰R¹¹,arylC₁-C₆alkyloxy, hetarylC₁-C₆alkyloxy, C₁-C₆alkylcarbonyl,arylcarbonyl, hetarylcarbonyl, arylC₁-C₆alkylcarbonyl,C₁-C₆alkyloxycarbonyl, aryloxycarbonyl or arylC₁-C₆alkyloxycarbonyl. 46.A compound according to claim 39, wherein R⁸ and R⁹ independently arehydrogen, C₁-C₆alkyl, hydroxy, oxo, C₁-C₆alkyloxy or arylC₁-C₆alkyloxy.47. A compound according to claim 39, wherein R¹⁰ and R¹¹ independentlyare hydrogen or C₁-C₈alkyl.
 48. A compound according to claim 39, whichis 1-(4-Chloro-phenyl)-5-propyl-1H-pyrazole-4-carboxylic acidcyclohexyl-methyl-amide, or a salt thereof with a pharmaceuticallyacceptable acid or base, or optical isomer or mixture of opticalisomers, racemic mixture, or tautomeric forms thereof.
 49. A compoundaccording to claim 39, selected from the group consisting of:1-(4-Chlorophenyl)-5-trifluoromethyl-1H-pyrazole-4-carboxylic acidcyclohexyl-methyl-amide;[1-(4-Methoxy-phenyl)-5-methyl-1H-pyrazol-4-yl]-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone;[1-(4-Chloro-phenyl)-5-propyl-1H-pyrazol-4-yl]-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone;and[1-(3,5-Dichloro-phenyl)-5-propyl-1H-pyrazol-4-yl]-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone;or a salt thereof with a pharmaceutically acceptable acid or base, oroptical isomer or mixture of optical isomers, racemic mixture, ortautomeric forms thereof.
 50. A compound according to claim 39, selectedfrom the group consisting of:1-(Phenyl)-5-methyl-1H-pyrazole-4-carboxylic acidcyclohexyl-methyl-amide;1-(4-Fluoro-phenyl)-5-methyl-1H-pyrazole-4-carboxylic acidcyclohexyl-methyl-amide;1-(4-Methoxy-phenyl)-5-methyl-1H-pyrazole-4-carboxylic acidcyclohexyl-methyl-amide;1-(4-Chloro-phenyl)-5-methyl-1H-pyrazole-4-carboxylic acidcyclohexyl-methyl-amide;1-(2-Methyl-phenyl)-5-methyl-1H-pyrazole-4-carboxylic acidcyclohexyl-methyl-amide;1-(4-Amino-phenyl)-5-methyl-1H-pyrazole-4-carboxylic acidcyclohexyl-methyl-amide; 1-(2-Pyridyl)-5-methyl-1H-pyrazole-4-carboxylicacid cyclohexyl-methyl-amide; and1-(2-Pyridyl)-5-propyl-1H-pyrazole-4-carboxylic acidcyclohexyl-methyl-amide; or a salt thereof with a pharmaceuticallyacceptable acid or base, or optical isomer or mixture of opticalisomers, racemic mixture, or tautomeric forms thereof.
 51. A compound offormula (IV):

wherein R¹ is hydrogen, trihalomethyl, C₁-C₆alkyl, C₁-C₆alkyloxy,C₁-C₆alkylthio, aryl, arylC₁-C₆alkyl, hetaryl or hetaralkyl, wherein thealkyl, aryl and hetaryl groups independently are optionally substitutedwith one or more of R⁸; R², R³, R⁴ and R⁵ independently are hydrogen,halo, nitro, cyano, hydroxy, NR⁹R¹⁰, trihalomethyl, C₁-C₆alkyl,C₁-C₆alkyloxy, C₁-C₆alkylthio, aryl, arylC₁-C₆alkyl, hetaryl orhetaralkyl, wherein the alkyl, aryl and hetaryl groups independently areoptionally substituted with one or more of R⁸; or R² together with R³are forming a saturated or partially saturated cyclic ring systemcontaining from 3 to 6 carbon atoms and from 0 to 2 additionalheteroatoms selected from nitrogen, oxygen or sulphur, the ring systemoptionally being substituted with at least one of C₁-C₆alkyl, aryl,hetaryl, arylC₁-C₆alkyl, hetarylC₁-C₆alkyl, hydroxy, oxo, C₁-C₆alkyloxy,aryloxy, arylC₁-C₆alkyloxy or hetarylC₁-C₆alkyloxy; or R³ together withR⁴ are forming a saturated or partially saturated cyclic ring systemcontaining from 3 to 6 carbon atoms and from 0 to 2 additionalheteroatoms selected from nitrogen, oxygen or sulphur, the ring systemoptionally being substituted with at least one of C₁-C₆alkyl, aryl,hetaryl, arylC₁-C₆alkyl, hetarylC₁-C₆alkyl, hydroxy, oxo, C₁-C₆alkyloxy,aryloxy, arylC₁-C₆alkyloxy or hetarylC₁-C₆alkyloxy; or R⁴ together withR⁵ are forming a saturated or partially saturated cyclic ring systemcontaining from 3 to 6 carbon atoms and from 0 to 2 additionalheteroatoms selected from nitrogen, oxygen or sulphur, the ring systemoptionally being substituted with at least one of C₁-C₆alkyl, aryl,hetaryl, arylC₁-C₆alkyl, hetarylC₁-C₆alkyl, hydroxy, oxo, C₁-C₆alkyloxy,aryloxy, arylC₁-C₆alkyloxy or hetarylC₁-C₆alkyloxy; R⁶ is aryl, hetaryl,arylC₁-C₆alkyl, C₃-C₁₀cycloalkyl, C₃-C₁₀hetcycloalkyl,C₃-C₁₀cycloalkylC₁-C₆alkyl, C₁-C₆alkylcarboxyC₁-C₆alkyl, wherein thealkyl, aryl and cycloalkyl groups independently are optionallysubstituted with one or more of R¹¹; R⁷ is C₁-C₈alkyl, aryl, hetaryl,arylC₁-C₆alkyl, C₃-C₁₀cycloalkyl, C₃-C₁₀hetcycloalkyl,C₃-C₁₀cycloalkylC₁-C₆alkyl, C₁-C₆alkylcarboxyC₁-C₆alkyl, wherein thealkyl, aryl and cycloalkyl groups independently are optionallysubstituted with one or more of R¹¹; or R⁶ and R⁷, together with thenitrogen to which they are attached, are forming a saturated orpartially saturated cyclic, bicyclic or tricyclic ring system containingfrom 6 to 10 carbon atoms and from 0 to 2 additional heteroatomsselected from nitrogen, oxygen or sulphur, the ring system optionallybeing substituted with at least one of C₁-C₈alkyl, aryl, hetaryl,arylC₁-C₆alkyl, hetarylC₁-C₆alkyl, hydroxy, oxo, cyano, C₁-C₆alkyloxy,arylC₁-C₆alkyloxy, hetarylC₁-C₆alkyloxy, C₁-C₆alkyloxyC₁-C₆alkyl,C₁-C₆alkylcarbonyl, arylcarbonyl, hetarylcarbonyl,arylC₁-C₆alkylcarbonyl, hetarylC₁-C₆alkylcarbonyl, C₁-C₆alkylcarboxy,arylcarboxy or arylC₁₋₆-alkylcarboxy wherein the alkyl and aryl groupsindependently are optionally substituted with one or more of R⁸; R⁹ andR¹⁰ independently are hydrogen, C₁-C₈alkyl, aryl, hetaryl,arylC₁-C₆alkyl, C₃-C₁₀-cycloalkyl, C₃-C₁₀hetcycloalkyl,C₃-C₁₀cycloalkylC₁-C₆alkyl, C₁-C₆alkylcarboxyC₁-C₆alkyl, wherein thealkyl, aryl and cycloalkyl groups independently are optionallysubstituted with one or more of R¹¹; or R⁹ and R¹⁰, together with thenitrogen to which they are attached, are forming a saturated orpartially saturated cyclic, bicyclic or tricyclic ring system containingfrom 4 to 10 carbon atoms and from 0 to 2 additional heteroatomsselected from nitrogen, oxygen or sulphur, the ring system optionallybeing substituted with at least one of C₁-C₈alkyl, aryl, hetaryl,arylC₁-C₆alkyl, hetarylC₁-C₆alkyl, hydroxy, oxo, cyano, C₁-C₆alkyloxy,arylC₁-C₆alkyloxy, hetarylC₁-C₆alkyloxy, C₁-C₆alkyloxyC₁-C₆alkyl,C₁-C₆alkylcarbonyl, arylcarbonyl, hetarylcarbonyl,arylC₁-C₆alkylcarbonyl, hetarylC₁-C₆alkylcarbonyl, C₁-C₆alkylcarboxy,arylcarboxy or arylC₁-C₆-alkylcarboxy wherein the alkyl and aryl groupsindependently are optionally substituted with one or more of R⁸; R⁸ andR¹¹ independently are hydrogen, halo, hydroxy, oxo, nitro, cyano,C₁-C₈alkyl, C₁-C₆-alkyloxy or aryloxy; or a salt thereof with apharmaceutically acceptable acid or base, or optical isomer or mixtureof optical isomers, racemic mixture, a prodrug thereof, or tautomericforms thereof.
 52. A compound according to claim 51, wherein R¹ ishydrogen or C₁-C₆alkyl, wherein the alkyl group is optionallysubstituted with one or more of R⁸.
 53. A compound according to claim51, wherein R², R³, R⁴ and R⁵ are hydrogen.
 54. A compound according toclaim 51, wherein R⁶ and R⁷, together with the nitrogen to which theyare attached, are forming a saturated or partially saturated cyclic,bicyclic or tricyclic ring system containing from 6 to 10 carbon atomsand from 0 to 2 additional nitrogen or oxygen atoms, the ring systemoptionally being substituted with at least one of C₁-C₈alkyl, aryl,hetaryl, arylC₁-C₆alkyl, hetarylC₁-C₆alkyl, hydroxy, oxo, cyano,C₁-C₆alkyloxy, arylC₁-C₆alkyloxy, hetarylC₁-C₆alkyloxy,C₁-C₆alkyloxyC₁-C₆alkyl, C₁-C₆alkylcarbonyl, arylcarbonyl,hetarylcarbonyl, arylC₁-C₆alkylcarbonyl, hetarylC₁-C₆alkylcarbonyl,C₁-C₆alkylcarboxy, arylcarboxy or arylC₁-C₆-alkylcarboxy wherein thealkyl and aryl groups independently are optionally substituted with oneor more of R⁸.
 55. A compound according to claim 51, which is:pyrazolo[1,5-a]pyridin-3-yl-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone;or a salt thereof with a pharmaceutically acceptable acid or base, oroptical isomer or mixture of optical isomers, racemic mixture, a prodrugthereof, or tautomeric forms thereof.
 56. A compound according to claim51, which is selected from:(2-Methyl-pyrazolo[1,5-a]pyridin-3-yl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone;and Pyrazolo[1,5-a]pyridine-3-carboxylic acid cyclohexyl-methyl-amide;or a salt thereof with a pharmaceutically acceptable acid or base, oroptical isomer or mixture of optical isomers, racemic mixture, ortautomeric forms thereof.
 57. A compound of formula (V):

wherein R¹ is hydrogen, C₁-C₈alkyl, C₁-C₆alkyloxyC₁-C₆alkyl, aryl,hetaryl, arylC₁-C₆alkyl, hetarylC₁-C₆alkyl, C₁-C₆SO₂, arylSO₂,hetarylSO₂, arylC₁-C₆alkylSO₂ or hetarylC₁-C₆alkylSO₂ optionallysubstituted with one or more R⁸; R² and R⁵ independently are hydrogen,halo, nitro, cyano, trihalomethyl, C₁-C₆alkyl, aryl, arylC₁-C₆alkyl,hetaryl or hetarylC₁-C₆alkyl wherein the alkyl, aryl, arylalkyl, hetaryland hetarylalkyl groups independently are substituted with one or moreR⁹; and either R³ is hydrogen; and R⁴ is C(O)NR⁷R⁸; or R³ is C(O)NR⁷R⁸;and R⁴ is hydrogen; R⁶ is hydrogen, halo, cyano, trihalomethyl, NR¹²R¹³,C₁-C₆alkyl, aryl, arylC₁-C₆alkyl, hetaryl or hetarylC₁-C₆alkyl whereinthe alkyl, aryl, arylalkyl, hetaryl and hetarylalkyl groupsindependently are substituted with one or more R⁹; and R⁷ and R⁸independently are C₁-C₈alkyl, C₃-C₁₀cycloalkyl, C₃-C₁₀hetcycloalkyl,C₃-C₁₀cycloalkylC₁-C₆alkyl, wherein the alkyl, cycloalkyl andhetcycloalkyl groups independently are optionally substituted with oneor more of R¹⁰; or R⁷ and R⁸ together with the nitrogen to which theyare attached, are forming a saturated or partially saturated bicyclic ortricyclic ring system containing from 6 to 10 carbon atoms and from 0 to2 additional heteroatoms selected from nitrogen or oxygen, the ringsystem optionally being substituted with at least one of C₁-C₈alkyl,arylC₁-C₆alkyl, hetarylC₁-C₆alkyl, hydroxy, cyano, C₁-C₆alkyloxy,arylC₁-C₆alkyloxy, hetarylC₁-C₆alkyloxy, C₁-C₆alkyloxyC₁-C₆alkyl,C₁-C₆alkylcarbonyl, arylcarbonyl, hetarylcarbonyl,arylC₁-C₆alkylcarbonyl, hetarylC₁-C₆alkylcarbonyl, C₁-C₆alkylcarboxy,arylcarboxy or arylC₁-C₆alkylcarboxy wherein the alkyl and aryl groupsindependently are optionally substituted with one or more of R¹¹; R⁹ ishydrogen, hydroxy, oxo, halo, nitro, cyano, C₁-C₆alkyl, C₁-C₆alkyloxy,trihalomethyl, trihalomethoxy, NR¹²R¹³, C(O)NR¹²R¹³, arylC₁-C₆alkyloxy,C₁-C₆alkylcarbonyl, arylcarbonyl, arylC₁-C₆alkylcarbonyl,C₁-C₆alkylcarboxy, arylcarboxy or arylC₁-C₆alkylcarboxy; R¹⁰ and R¹¹independently are hydrogen, halo, oxo, hydroxy, C₁-C₆alkyl, aryl,arylC₁-C₆alkyl, hetaryl or hetarylalkyl; R¹² and R¹³ independently arehydrogen, C₁-C₈alkyl, aryl, hetaryl, arylC₁-C₆alkyl, C₃-C₁₀-cycloalkyl,C₃-C₁₀hetcycloalkyl, C₃-C₁₀cycloalkylC₁-C₆alkyl, C₁-C₆alkylcarbonyl,arylcarbonyl, arylC₁-C₈alkylcarbonyl, hetarylcarbonyl,hetarylC₁-C₆alkylcarbonyl, C₁-C₆alkylcarboxyC₁-C₆alkyl; or R¹² and R¹³together with the nitrogen to which they are attached, are forming asaturated or partially saturated cyclic, bicyclic or tricyclic ringsystem containing from 4 to 10 carbon atoms and from 0 to 2 additionalheteroatoms selected from nitrogen, oxygen or sulphur, the ring systemoptionally being substituted with at least one of C₁-C₈alkyl, aryl,hetaryl, arylC₁-C₆alkyl, hetarylC₁-C₆alkyl, hydroxy, oxo, cyano,C₁-C₆alkyloxy, arylC₁-C₆alkyloxy, hetarylC₁-C₆alkyloxy,C₁-C₆alkyl-oxyC₁-C₆alkyl, C₁-C₆alkylcarbonyl, arylcarbonyl,hetarylcarbonyl, arylC₁-C₆alkylcarbonyl, hetarylC₁-C₆alkylcarbonyl,C₁-C₆alkylcarboxy, arylcarboxy or arylC₁-C₆alkylcarboxy; or a saltthereof with a pharmaceutically acceptable acid or base, or opticalisomer or mixture of optical isomers, racemic mixture, a prodrugthereof, or tautomeric forms thereof.
 58. A compound according to claim57, of formula (Va):

wherein R¹ is hydrogen, C₁-C₈alkyl, aryl, hetaryl, arylC₁-C₆alkyl orhetarylC₁-C₆alkyl optionally substituted with one or more R⁸; R² and R⁵independently are hydrogen, halo, nitro, cyano, trihalomethyl,C₁-C₆alkyl, aryl, arylC₁-C₆alkyl, hetaryl or hetarylC₁-C₆alkyl whereinthe alkyl, aryl, arylalkyl, hetaryl and hetarylalkyl groupsindependently are substituted with one or more R⁸; and either R³ ishydrogen; and R⁴ is C(O)NR⁶R⁷; or R³ is C(O)NR⁶R⁷; and R⁴ is hydrogen;R⁶ and R⁷ independently are C₁-C₈alkyl, C₃-C₁₀cycloalkyl,C₃-C₁₀hetcycloalkyl, C₃-C₁₀cycloalkylC₁-C₆alkyl, wherein the alkyl,cycloalkyl and hetcycloalkyl groups independently are optionallysubstituted with one or more of R⁹; or R⁶ and R⁷ together with thenitrogen to which they are attached, are forming a saturated orpartially saturated bicyclic or tricyclic ring system containing from 6to 10 carbon atoms and from 0 to 2 additional heteroatoms selected fromnitrogen or oxygen, the ring system optionally being substituted with atleast one of C₁-C₈alkyl, arylC₁-C₆alkyl, hetarylC₁-C₆alkyl, hydroxy,cyano, C₁-C₆alkyloxy, arylC₁-C₆alkyloxy, hetarylC₁-C₆alkyloxy,C₁-C₆alkyloxyC₁-C₆alkyl, C₁-C₆alkylcarbonyl, arylcarbonyl,hetarylcarbonyl, arylC₁-C₆alkylcarbonyl, hetarylC₁-C₆alkylcarbonyl,C₁-C₆alkylcarboxy, arylcarboxy or arylC₁-C₆alkylcarboxy wherein thealkyl and aryl groups independently are optionally substituted with oneor more of R¹⁰; R⁸ is hydrogen, hydroxy, oxo, halo, nitro, cyano,C₁-C₆alkyl, C₁-C₆alkyloxy, trihalomethyl, trihalomethoxy, NR¹¹R¹²,arylC₁-C₆alkyloxy, C₁-C₆alkylcarbonyl, arylcarbonyl,arylC₁-C₆alkylcarbonyl, C₁-C₆alkylcarboxy, arylcarboxy orarylC₁-C₆alkylcarboxy; R⁹ and R¹⁰ independently are hydrogen, halo, oxo,hydroxy, C₁-C₆alkyl, aryl, arylC₁-C₆alkyl, hetaryl or hetarylalkyl; R¹¹and R¹² independently are hydrogen, C₁-C₈alkyl, aryl, hetaryl,arylC₁-C₆alkyl, C₃-C₁₀-cycloalkyl, C₃-C₁₀hetcycloalkyl,C₃-C₁₀cycloalkylC₁-C₆alkyl, C₁-C₆alkyl-carboxyC₁-C₆alkyl; or R¹¹ and R¹²together with the nitrogen to which they are attached, are forming asaturated or partially saturated cyclic, bicyclic or tricyclic ringsystem containing from 4 to 10 carbon atoms and from 0 to 2 additionalheteroatoms selected from nitrogen, oxygen or sulphur, the ring systemoptionally being substituted with at least one of C₁-C₈alkyl, aryl,hetaryl, arylC₁-C₆alkyl, hetarylC₁-C₆alkyl, hydroxy, oxo, cyano,C₁-C₆alkyloxy, arylC₁-C₆alkyloxy, hetarylC₁-C₆alkyloxy,C₁-C₆alkyl-oxyC₁-C₆alkyl, C₁-C₆alkylcarbonyl, arylcarbonyl,hetarylcarbonyl, arylC₁-C₆alkyl-carbonyl, hetarylC₁-C₆alkylcarbonyl,C₁-C₆alkylcarboxy, arylcarboxy or arylC₁-C₆alkylcarboxy; or a saltthereof with a pharmaceutically acceptable acid or base, or opticalisomer or mixture of optical isomers, racemic mixture, a prodrugthereof, or tautomeric forms thereof.
 59. A compound according to claim57, wherein R¹ is hydrogen, C₁-C₈alkyl, arylC₁-C₆alkyl,hetarylC₁-C₆alkyl, arylSO₂, hetarylSO₂, arylC₁-C₆alkylSO₂ orhetarylC₁-C₆alkylSO₂ all of which is optionally substituted with one ormore R⁸.
 60. A compound according to claim 57, wherein R² and R⁵ arehydrogen.
 61. A compound according to claim 57, wherein R³ is hydrogenand R⁴ is C(O)NR⁷R⁸.
 62. A compound according to claim 57, wherein R³ isC(O)NR⁷R⁸ and R⁴ is hydrogen.
 63. A compound according to claim 57,wherein R⁶ is hydrogen, NR¹²R¹³, C₁-C₆alkyl, aryl or hetaryl wherein thealkyl, aryl and hetaryl independently are substituted with one or moreR⁹.
 64. A compound according to claim 57, wherein R⁷ and R⁸independently are C₁-C₈alkyl or C₃-C₁₀cycloalkyl, wherein the alkyl andcycloalkyl groups independently are optionally substituted with one ormore of R¹⁰.
 65. A compound according to claim 57, wherein R⁹ ishydrogen, hydroxy, oxo, halo, nitro, cyano, C₁-C₆alkyl, C₁-C₆alkyloxy,trihalomethyl, trihalomethoxy, NR¹²R¹³, C(O)NR¹²R¹³, arylC₁-C₆alkyloxy,C₁-C₆alkylcarbonyl, arylcarbonyl, arylC₁-C₆alkylcarbonyl.
 66. A compoundaccording to claim 57, wherein R¹⁰ and R¹¹ independently are hydrogen,halo, oxo, hydroxy, C₁-C₆alkyl, aryl, arylC₁-C₆alkyl, hetaryl orhetarylalkyl.
 67. A compound according to claim 57, which is:1H-Benzoimidazole-5-carboxylic acid cyclohexyl-methyl-amide, or a saltthereof with a pharmaceutically acceptable acid or base, or opticalisomer or mixture of optical isomers, racemic mixture, a prodrugthereof, or tautomeric forms thereof.
 68. A compound according to claim57, selected from the group consisting of:1-Benzyl-1H-benzoimidazole-5-carboxylic acid cyclohexyl-methyl-amide;and(1H-Benzoimidazol-5-yl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone;or a salt thereof with a pharmaceutically acceptable acid or base, oroptical isomer or mixture of optical isomers, racemic mixture, a prodrugthereof, or tautomeric forms thereof.
 69. A compound according to claim57, selected from the group consisting of:Isopropyl-2-trifluoromethyl-1H-benzoimidazole-5-carboxylic acidcyclohexyl-methyl-amide; 1-Benzyl-1H-benzoimidazole-5-carboxylic acidcyclohexyl-methyl-amide; 2-Methyl-1H-benzoimidazole-5-carboxylic acidcyclohexyl-methyl-amide; 2-Hydroxymethyl-1H-benzoimidazole-5-carboxylicacid cyclohexyl-methyl-amide;2-(4-Amino-phenyl)-1H-benzoimidazole-5-carboxylic acidcyclohexyl-methyl-amide;(1H-Benzoimidazol-5-yl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone;(2-Methyl-1H-benzoimidazol-5-yl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone;(2-Amino-1H-benzoimidazol-5-yl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone;(2-Benzo[1,3]dioxol-5-yl-1H-benzoimidazol-5-yl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone;3-[5-(1,3,3-Trimethyl-6-aza-bicyclo[3.2.1]octane-6-carbonyl)-1H-benzoimidazol-2-yl]-benzoicacid methyl ester;(2-Thiophen-2-yl-1H-benzoimidazol-5-yl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone;and[2-(2-Nitro-phenyl)-1H-benzoimidazol-5-yl]-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone;or a salt thereof with a pharmaceutically acceptable acid or base, oroptical isomer or mixture of optical isomers, racemic mixture, a prodrugthereof, or tautomeric forms thereof.
 70. A compound of formula (VI):

wherein X is oxygen or (CR¹R²)_(n); R¹, R², R³, and R⁴ independently arehydrogen, C₁-C₆alkyl, aryl, arylC₁-C₆alkyl, hetaryl or hetarylC₁-C₆alkyloptionally substituted with one or more R⁸ independently; or R¹ andeither R³ or R⁴ together are forming a saturated or partially saturatedring system containing from 4 to 8 carbon atoms, the ring systemoptionally being substituted with at least one of C₁-C₆alkyl, hydroxy,oxo, aryl, hetaryl, arylC₁-C₆alkyl or hetarylC₁-C₆alkyl; or R¹ andeither R³ or R⁴ together with the single bond are forming acarbon-carbon double bond; R⁵ is C₁-C₈alkyl optionally substituted withone or more of R⁹; R⁶ is C₃-C₁₀cycloalkyl, C₃-C₁₀hetcycloalkyl,C₃-C₁₀cycloalkylC₁-C₆alkyl, wherein the alkyl, cycloalkyl andhetcycloalkyl groups independently are optionally substituted with oneor more of R⁹; or R⁵ and R⁶ together with the nitrogen to which they areattached, are forming a saturated or partially saturated cyclic,bicyclic or tricyclic ring system containing from 6 to 10 carbon atomsand from 0 to 2 additional heteroatoms selected from nitrogen, oxygen orsulphur, the ring system optionally being substituted with at least oneof C₁-C₆alkyl, aryl, hetaryl, arylC₁-C₆alkyl, hetarylC₁-C₆alkyl,hydroxy, oxo, cyano, C₁-C₆alkyloxy, arylC₁-C₆alkyloxy,hetarylC₁-C₆alkyloxy, C₁-C₆alkyloxyC₁-C₆alkyl, C₁-C₆alkylcarbonyl,arylcarbonyl, hetarylcarbonyl, arylC₁-C₆alkylcarbonyl,hetarylC₁-C₆alkylcarbonyl, C₁-C₆alkylcarboxy, arylcarboxy orarylC₁-C₆alkylcarboxy wherein the alkyl and aryl groups independentlyare optionally substituted with one or more of R¹⁰; R⁷ is hydrogen,halo, nitro, NR¹²R¹³, cyano, trihalomethyl, C₁-C₆alkyl, aryl,arylC₁-C₆alkyl, C₁-C₆alkyloxy, aryloxy, arylC₁-C₆alkyloxy, hetaryl,hetarylC₁-C₆alkyl, hetaryloxy or hetarylC₁-C₆-alkyloxy optionallysubstituted with one or more R¹¹ independently; R⁸ and R⁹ independentlyare hydrogen, hydroxy, oxo, halo, nitro, cyano, C₁-C₆alkyl,C₁-C₆-alkyloxy, trihalomethyl, trihalomethoxy, NR¹²R¹³,arylC₁-C₆alkyloxy, C₁-C₆alkylcarbonyl, arylcarbonyl,arylC₁-C₆alkylcarbonyl, C₁-C₆alkylcarboxy, arylcarboxy orarylC₁-C₆alkylcarboxy; R¹⁰ is hydrogen, C₁-C₈alkyl, arylC₁-C₆alkyl,hetarylC₁-C₆alkyl, C₁-C₆alkyloxy, arylC₁-C₆alkyloxy,hetarylC₁-C₆alkyloxy; R¹¹ is hydrogen, halo, hydroxy, oxo, nitro, cyano,C₁-C₈alkyl, C₁-C₆alkyloxy, aryloxy or hetaryloxy; R¹² and R¹³independently are hydrogen, C₁-C₈alkyl, aryl, hetaryl, arylC₁-C₆alkyl,C₃-C₁₀cycloalkyl, C₃-C₁₀hetcycloalkyl, C₁-C₆alkylcarbonyl,arylC₁-C₆alkylcarbonyl, C₃-C₁₀cycloalkylC₁-C₆-alkyl,C₁-C₆alkyloxycarbonyl; or R¹² and R¹³ are together with the nitrogen towhich they are attached, are forming a saturated or partially saturatedcyclic, bicyclic or tricyclic ring system containing from 4 to 10 carbonatoms and from 0 to 2 additional heteroatoms selected from nitrogen,oxygen or sulphur, the ring system optionally being substituted with atleast one of C₁-C₆alkyl, aryl, hetaryl, arylC₁-C₆alkyl,hetarylC₁-C₆alkyl, hydroxy, oxo, cyano, C₁-C₆alkyloxy,arylC₁-C₆alkyloxy, hetarylC₁-C₆alkyloxy, C₁-C₆alkyloxyC₁-C₆alkyl,C₁-C₆alkylcarbonyl, arylcarbonyl, hetarylcarbonyl,arylC₁-C₆alkylcarbonyl, hetarylC₁-C₆alkylcarbonyl, C₁-C₆alkylcarboxy,arylcarboxy or arylC₁₋₆alkylcarboxy; n is 1 or 2; or a salt thereof witha pharmaceutically acceptable acid or base, or optical isomer or mixtureof optical isomers, racemic mixture, a prodrug thereof, or tautomericforms thereof.
 71. A compound according to claim 70, wherein X is(CR¹R²)_(n).
 72. A compound according to claim 70, wherein X is oxygen.73. A compound according to claim 70, wherein R¹, R², R³, and R⁴independently are hydrogen, C₁-C₆alkyl or arylC₁-C₆alkyl, optionallysubstituted with one or more R⁸.
 74. A compound according to claim 70,wherein R¹ and either R³ or R⁴ together with the single bond are forminga carbon-carbon double bond.
 75. A compound according to claim 70,wherein R⁵ is C₁-C₈alkyl optionally substituted with one or more of R⁹.76. A compound according to claim 70, wherein R⁶ is C₃-C₁₀cycloalkyl orC₃-C₁₀hetcycloalkyl, each of which is optionally substituted with one ormore of R⁹.
 77. A compound according to claim 70, wherein R⁵ and R⁶together with the nitrogen to which they are attached, are forming asaturated or partially saturated cyclic, bicyclic or tricyclic ringsystem containing from 6 to 10 carbon atoms and from 0 to 2 additionalheteroatoms selected from nitrogen, oxygen or sulphur, the ring systemoptionally being substituted with at least one of C₁-C₆alkyl, aryl,hetaryl, arylC₁-C₆alkyl, hetarylC₁-C₆alkyl, hydroxy, oxo, cyano,C₁-C₆alkyloxy, arylC₁-C₆alkyloxy, hetarylC₁-C₆alkyloxy,C₁-C₆alkyloxyC₁-C₆alkyl, C₁-C₆alkylcarbonyl, arylcarbonyl,hetarylcarbonyl, arylC₁-C₆alkylcarbonyl, hetarylC₁-C₆alkylcarbonyl,C₁-C₆alkylcarboxy, arylcarboxy or arylC₁-C₆alkylcarboxy wherein thealkyl and aryl groups independently are optionally substituted with oneor more of R¹⁰.
 78. A compound according to claim 70, wherein R⁷ ishydrogen, halo, NR¹²R¹³, trihalomethyl, C₁-C₆alkyloxy, aryloxy,arylC₁-C₆alkyloxy, hetaryloxy optionally substituted with one or moreR¹¹ independently.
 79. A compound according to claim 70, wherein R⁸ andR⁹ independently are hydrogen, hydroxy, oxo, halo, nitro, cyano,C₁-C₆alkyl, C₁-C₆alkyloxy, trihalomethyl or NR¹²R¹³.
 80. A compoundaccording to claim 70, wherein R¹⁰ is hydrogen or C₁-C₈alkyl.
 81. Acompound according to claim 70, selected from the group consisting of:2,3-Dimethyl-2,3-dihydro-benzofuran-7-carboxylic acidcyclohexyl-methyl-amide; 2,5-Dimethyl-3-phenyl-benzofuran-7-carboxylicacid cyclohexyl-methyl-amide;2,2-Dimethyl-2,3-dihydro-benzofuran-7-carboxylic acidcyclohexyl-methyl-amide; 2-Methyl-2,3-dihydro-benzofuran-7-carboxylicacid cyclohexyl-methyl-amide;(2,3-Dimethyl-2,3-dihydro-benzofuran-7-yl)-(2,4,4-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone;4-Methoxy-2-methyl-2,3-dihydro-benzofuran-7-carboxylic acidcyclohexyl-methyl-amide; 2-Methyl-benzofuran-7-carboxylic acidcyclohexyl-methyl-amide;(2-Methyl-2,3-dihydro-benzofuran-7-yl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone;Benzofuran-7-carboxylic acid cyclohexyl-methyl-amide;2,3-Dihydro-benzofuran-7-carboxylic acid cyclohexyl-methyl-amide;3,3-Dimethyl-2,3-dihydro-benzofuran-7-carboxylic acidcyclohexyl-methyl-amide; and Chroman-8-carboxylic acidcyclohexyl-methyl-amide; or a salt thereof with a pharmaceuticallyacceptable acid or base, or optical isomer or mixture of opticalisomers, racemic mixture, a prodrug thereof, or tautomeric formsthereof.
 82. A compound according to claim 70, selected from the groupconsisting of: 2,3-Dihydro-benzofuran-7-carboxylic acidcyclohexyl-methyl-amide; Benzofuran-7-carboxylic acidcyclohexyl-methyl-amide; 2-Methyl-2,3-dihydro-benzofuran-7-carboxylicacid cyclohexyl-methyl-amide; 2-Methyl-benzofuran-7-carboxylic acidcyclohexyl-methyl-amide;3,3-Dimethyl-2,3-dihydro-benzofuran-7-carboxylic acidcyclohexyl-methyl-amide;(2,3-Dimethyl-2,3-dihydro-benzofuran-7-yl)-(2,4,4-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone;4-Methoxy-2-methyl-2,3-dihydro-benzofuran-7-carboxylic acidcyclohexyl-methyl-amide;2,2-Dimethyl-2,3-dihydro-benzofuran-7-carboxylic acidcyclohexyl-methyl-amide;(2-Methyl-2,3-dihydro-benzofuran-7-yl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone;and Chroman-8-carboxylic acid cyclohexyl-methyl-amide; or a salt thereofwith a pharmaceutically acceptable acid or base, or optical isomer ormixture of optical isomers, racemic mixture, a prodrug thereof, ortautomeric forms thereof.
 83. A compound of formula (VII):

wherein R¹ is hydrogen, C₁-C₈alkyl, hetaryl, arylC₁-C₆alkyl orhetarylC₁-C₆alkyl optionally substituted with one or more R⁹; R², R³,R⁴, R⁵ and R⁶ independently are hydrogen, halo, nitro, cyano,trihalomethyl, carboxy, N(R¹²R¹³), C(O)NR⁷R⁸, C₁-C₈alkyl,C₃-C₁₀cycloalkyl, C₃-C₁₀hetcycloalkyl, N(R¹²R¹³)C₁-C₆alkyl,C₁-C₆alkylcarboxy, arylcarboxy, arylC₁-C₆alkylcarboxy, C₁-C₆alkyloxy,C₁-C₆alkyloxyC₁-C₆alkyl, aryl, arylC₁-C₆alkyl, aryloxy,aryloxyC₁-C₆alkyl, arylC₁-C₆alkyloxy, arylC₁-C₆alkyl-oxyC₁-C₆alkyl,hetaryl, hetarylC₁-C₆alkyl, hetarylC₁-C₆alkyloxy, hetaryloxyC₁-C₆alkylor hetarylC₁-C₆alkyloxyC₁-C₆alkyl wherein the alkyl, aryl, arylalkyl,hetaryl and hetarylalkyl groups independently are substituted with oneor more R⁹; R⁷ is hydrogen or C₁-C₈alkyl optionally substituted with oneor more of R¹⁰; R⁸ is C₃-C₁₀cycloalkyl, C₃-C₁₀hetcycloalkyl,C₃-C₁₀cycloalkylC₁-C₆alkyl, wherein the cycloalkyl and hetcycloalkylgroups independently are optionally substituted with one or more of R¹⁰;or R⁷ and R⁸ together with the nitrogen to which they are attached, areforming a saturated or partially saturated cyclic, bicyclic or tricyclicring system containing from 4 to 10 carbon atoms and from 0 to 2additional heteroatoms selected from nitrogen or oxygen, the ring systemoptionally being substituted with at least one of C₁-C₈alkyl, aryl,hetaryl, arylC₁-C₆alkyl, hetarylC₁-C₆alkyl, hydroxy, oxo, cyano,C₁-C₆alkyloxy, arylC₁-C₆alkyloxy, hetarylC₁-C₆alkyl-oxy,C₁-C₆alkyloxyC₁-C₆alkyl, C₁-C₆alkylcarbonyl, arylcarbonyl,hetarylcarbonyl, arylC₁-C₆alkylcarbonyl, hetarylC₁-C₆alkylcarbonyl,C₁-C₆alkylcarboxy, arylcarboxy or arylC₁-C₆alkylcarboxy wherein thealkyl and aryl groups independently are optionally substituted with oneor more of R¹¹; R⁹ is hydrogen, hydroxy, oxo, halo, nitro, cyano,C₁-C₆alkyl, C₁-C₆alkyloxy, trihalomethyl, trihalomethoxy, NR¹²R¹³,arylC₁-C₆alkyloxy, C₁-C₆alkylcarbonyl, arylcarbonyl,arylC₁-C₆alkylcarbonyl, C₁-C₆alkylcarboxy, arylcarboxy orarylC₁-C₆alkylcarboxy; R¹⁰ and R¹¹ independently are hydrogen, halo,oxo, hydroxy, C₁-C₆alkyl, aryl, arylC₁-C₆alkyl, hetaryl or hetarylalkyl;R¹² and R¹³ independently are hydrogen, C₁-C₈alkyl, aryl, hetaryl,arylC₁-C₆alkyl, C₃-C₁₀-cycloalkyl, C₃-C₁₀hetcycloalkyl,C₃-C₁₀cycloalkylC₁-C₆alkyl, C₁-C₆alkylcarbonyl, arylcarbonyl,arylC₁-C₆alkylcarbonyl, C₃-C₁₀cycloalkylcarbonyl,C₃-C₁₀hetcycloalkylcarbonyl or C₃-C₁₀cycloalkylC₁-C₆alkylcarbonylwherein the alkyl and aryl groups independently are optionallysubstituted with one or more of R¹¹, wherein R¹¹ is as defined above; orR¹² and R¹³ together with the nitrogen to which they are attached, areforming a saturated or partially saturated cyclic, bicyclic or tricyclicring system containing from 4 to 10 carbon atoms and from 0 to 2additional heteroatoms selected from nitrogen, oxygen or sulphur, thering system optionally being substituted with at least one ofC₁-C₈alkyl, aryl, hetaryl, arylC₁-C₆alkyl, hetarylC₁-C₆alkyl, hydroxy,oxo, cyano, C₁-C₆alkyloxy, arylC₁-C₆alkyloxy, hetarylC₁-C₆alkyloxy,C₁-C₆alkyl-oxyC₁-C₆alkyl, C₁-C₆alkylcarbonyl, arylcarbonyl,hetarylcarbonyl, arylC₁-C₆alkylcarbonyl, hetarylC₁-C₆alkylcarbonyl,C₁-C₆alkylcarboxy, arylcarboxy or arylC₁-C₆alkylcarboxy; or a saltthereof with a pharmaceutically acceptable acid or base, or opticalisomer or mixture of optical isomers, racemic mixture, a prodrugthereof, or tautomeric forms thereof.
 84. A compound according to claim83, wherein R¹ is hydrogen, C₁-C₈alkyl, hetaryl, arylC₁-C₆alkyl orhetarylC₁-C₆alkyl optionally substituted with one or more R⁹; R² and R⁵independently are hydrogen, halo, nitro, cyano, trihalomethyl,C₁-C₆alkyl, C₁-C₆-alkyloxy, C₁-C₆alkyloxyC₁-C₆alkyl, aryl,arylC₁-C₆alkyl, aryloxy, aryloxyC₁-C₆alkyl, arylC₁-C₆-alkyloxy,arylC₁-C₆alkyloxyC₁-C₆alkyl, hetaryl or hetarylC₁-C₆alkyl wherein thealkyl, aryl, arylalkyl, hetaryl and hetarylalkyl groups independentlyare substituted with one or more R⁹; and either R³ is C(O)NR⁷R⁸, and R⁴is hydrogen; or R³ is hydrogen, and R⁴ is C(O)NR⁷R⁸; R⁶ is C₁-C₈alkyl,C₃-C₁₀cycloalkyl, C₃-C₁₀hetcycloalkyl, N(R¹²R¹³)C₁-C₆alkyl,C₁-C₆alkyloxyC₁-C₆-alkyl, aryloxyC₁-C₆alkyl, arylC₁-C₆alkyloxy orarylC₁-C₆alkyloxyC₁-C₆alkyl; R⁷ is C₁-C₈alkyl optionally substitutedwith one or more of R¹⁰; R⁸ is C₃-C₁₀cycloalkyl, C₃-C₁₀hetcycloalkyl,C₃-C₁₀cycloalkylC₁-C₆alkyl, wherein the cycloalkyl and hetcycloalkylgroups independently are optionally substituted with one or more of R¹⁰;or R⁷ and R⁸ together with the nitrogen to which they are attached, areforming a saturated or partially saturated cyclic, bicyclic or tricyclicring system containing from 6 to 10 carbon atoms and from 0 to 2additional heteroatoms selected from nitrogen or oxygen, the ring systemoptionally being substituted with at least one of C₁-C₈alkyl, aryl,hetaryl, arylC₁-C₆alkyl, hetarylC₁-C₆alkyl, hydroxy, oxo, cyano,C₁-C₆alkyloxy, arylC₁-C₆alkyloxy, hetarylC₁-C₆alkyl-oxy,C₁-C₆alkyloxyC₁-C₆alkyl, C₁-C₆alkylcarbonyl, arylcarbonyl,hetarylcarbonyl, arylC₁-C₆alkylcarbonyl, hetarylC₁-C₆alkylcarbonyl,C₁-C₆alkylcarboxy, arylcarboxy or arylC₁-C₆alkylcarboxy wherein thealkyl and aryl groups independently are optionally substituted with oneor more of R¹¹; R⁹ is hydrogen, hydroxy, oxo, halo, nitro, cyano,C₁-C₆alkyl, C₁-C₆alkyloxy, trihalomethyl, trihalomethoxy, NR¹²R¹³,arylC₁-C₆alkyloxy, C₁-C₆alkylcarbonyl, arylcarbonyl,arylC₁-C₆alkylcarbonyl, C₁-C₆alkylcarboxy, arylcarboxy orarylC₁-C₆alkylcarboxy; R¹⁰ and R¹¹ independently are hydrogen, halo,oxo, hydroxy, C₁-C₆alkyl, aryl, arylC₁-C₆alkyl, hetaryl or hetarylalkyl;R¹² and R¹³ independently are hydrogen, C₁-C₈alkyl, aryl, hetaryl,arylC₁-C₆alkyl, C₃-C₁₀-cycloalkyl, C₃-C₁₀hetcycloalkyl,C₃-C₁₀cycloalkylC₁-C₆alkyl, C₁-C₆alkylcarbonyl, arylcarbonyl,arylC₁-C₆alkylcarbonyl, C₃-C₁₀cycloalkylcarbonyl,C₃-C₁₀hetcycloalkylcarbonyl or C₃-C₁₀cycloalkylC₁-C₆alkylcarbonyl; orR¹² and R¹³ together with the nitrogen to which they are attached, areforming a saturated or partially saturated cyclic, bicyclic or tricyclicring system containing from 4 to 10 carbon atoms and from 0 to 2additional heteroatoms selected from nitrogen, oxygen or sulphur, thering system optionally being substituted with at least one ofC₁-C₈alkyl, aryl, hetaryl, arylC₁-C₆alkyl, hetarylC₁-C₆alkyl, hydroxy,oxo, cyano, C₁-C₆alkyloxy, arylC₁-C₆alkyloxy, hetarylC₁-C₆alkyloxy,C₁-C₆alkyl-oxyC₁-C₆alkyl, C₁-C₆alkylcarbonyl, arylcarbonyl,hetarylcarbonyl, arylC₁-C₆alkylcarbonyl, hetarylC₁-C₆alkylcarbonyl,C₁-C₆alkylcarboxy, arylcarboxy or arylC₁-C₆alkylcarboxy; or a saltthereof with a pharmaceutically acceptable acid or base, or opticalisomer or mixture of optical isomers, racemic mixture, or tautomericforms thereof.
 85. A compound according to claim 83, wherein R² isC(O)NR⁷R⁸ and R³, R⁴, and R⁵ are hydrogen.
 86. A compound according toclaim 83, wherein R³ is C(O)NR⁷R⁸ and R⁴ is hydrogen.
 87. A compoundaccording to claim 83, wherein R⁴ is C(O)NR⁷R⁸ and R³ is hydrogen.
 88. Acompound according to 83, wherein R⁵ is C(O)NR⁷R⁸ and R², R³, and R⁴ arehydrogen.
 89. A compound according to claim 83, wherein R⁶ is C(O)NR⁷R⁸.90. A compound according to claim 83, selected from the group consistingof:(1H-Indol-5-yl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone;and 1H-Indole-6-carboxylic acid cyclohexyl-methyl-amide; or a saltthereof with a pharmaceutically acceptable acid or base, or opticalisomer or mixture of optical isomers, racemic mixture, a prodrugthereof, or tautomeric forms thereof.
 91. A compound according to claim83, selected from the group consisting of:(1H-Indol-7-yl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone;(1H-Indol-6-yl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone;1H-Indole-6-carboxylic acid adamantan-2-ylamide;(6-Aza-bicyclo[3.2.1]oct-6-yl)-(1H-indol-6-yl)-methanone;1H-Indole-6-carboxylic acid(8-methyl-8-aza-bicyclo[3.2.1]oct-3-yl)-amide; 1H-Indole-5-carboxylicacid adamantan-2-ylamide;(6-Aza-bicyclo[3.2.1]oct-6-yl)-(1H-indol-5-yl)-methanone;(1H-Indol-4-yl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone;(1H-Indol-3-yl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone;(1H-Indol-2-yl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone;(1-Methyl-1H-indol-3-yl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone;(3-Aza-bicyclo[3.2.2]non-3-yl)-(1H-indol-3-yl)-methanone;1-Methyl-1H-indole-3-carboxylic acid cycloheptylamide;1-Methyl-1H-indole-3-carboxylic acid adamantan-1-ylamide;(3-Aza-bicyclo[3.2.2]non-3-yl)-(1-methyl-1H-indol-3-yl)-methanone;(1-Methyl-1H-indol-3-yl)-(4-methyl-piperazin-1-yl)-methanone;1-Methyl-1H-indole-3-carboxylic acid (3-hydroxy-adamantan-1-yl)-amide;1-Methyl-1H-indole-3-carboxylic acid azepan-1-ylamide;1-Methyl-1H-indole-3-carboxylic acid (2-oxo-azepan-3-yl)-amide;(4-Benzyl-piperidine-1-yl)-(1-methyl-1H-indol-3-yl)-methanone;1-Methyl-1H-indole-3-carboxylic acid(2,6-dimethyl-piperidin-1-yl)-amide; 1-Methyl-1H-indole-3-carboxylicacid (2-methyl-piperidin-1-yl)-amide;(1-Cyclopropylmethyl-6-fluoro-1H-indol-3-yl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone;Azepan-1-yl-(1-methyl-1H-indol-3-yl)-methanone;(5-Benzyloxy-1H-indol-3-yl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone;(5H-[1,3]Dioxolo[4,5]indol-7-yl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone;(5-Chloro-1H-indol-3-yl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone;(6-Trifluoromethyl-1H-indol-3-yl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone;(6-Methyl-1H-indol-3-yl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone;(6-Nitro-1H-indol-3-yl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone;(5-Methoxy-1H-indol-3-yl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone;(6-Fluoro-1H-indol-3-yl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone;(6-Methoxy-1H-indol-3-yl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone;(7-Nitro-1H-indol-3-yl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone;(1H-Indol-4-yl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone;2-(1H-Indol-3-yl)-1-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-ethanone;1-(3-Aza-bicyclo[3.2.2]non-3-yl)-2-(1H-indol-3-yl)-ethanone;1-(3-Aza-bicyclo[3.2.2]non-3-yl)-2-(1-methyl-1H-indol-3-yl)-ethanone;2-(1-Methyl-1H-indol-3-yl)-1-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-ethanone;[3-(1,3,3-Trimethyl-6-aza-bicyclo[3.2.1]octane-6-carbonyl)-1H-indol-6-yloxy]-aceticacid tert-butyl ester;6-(1,3,3-Trimethyl-6-aza-bicyclo[3.2.1]octane-6-carbonyl)-1H-indole-3-carboxylicacid;6-(1,3,3-Trimethyl-6-aza-bicyclo[3.2.1]octane-6-carbonyl)-1H-indole-3-carboxylicacid ethyl ester;5-(1,3,3-Trimethyl-6-aza-bicyclo[3.2.1]octane-6-carbonyl)-1H-indole-3-carboxylicacid;5-(1,3,3-Trimethyl-6-aza-bicyclo[3.2.1]octane-6-carbonyl)-1H-indole-3-carboxylicacid ethyl ester;4-(1,3,3-Trimethyl-6-aza-bicyclo[3.2.1]octane-6-carbonyl)-1H-indole-3-carboxylicacid;4-(1,3,3-Trimethyl-6-aza-bicyclo[3.2.1]octane-6-carbonyl)-1H-indole-3-carboxylicacid ethyl ester;5-(1,3,3-Trimethyl-6-aza-bicyclo[3.2.1]octane-6-carbonyl)-1H-indole-3-carboxylicacid;5-(1,3,3-Trimethyl-6-aza-bicyclo[3.2.1]octane-6-carbonyl)-1H-indole-3-carboxylicacid ethyl ester;4-(1,3,3-Trimethyl-6-aza-bicyclo[3.2.1]octane-6-carbonyl)-1H-indole-3-carboxylicacid;4-(1,3,3-Trimethyl-6-aza-bicyclo[3.2.1]octane-6-carbonyl)-1H-indole-3-carboxylicacid ethyl ester;[3-(Piperidine-1-carbonyl)-1H-indol-5-yl]-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone;5-(1,3,3-Trimethyl-6-aza-bicyclo[3.2.1]octane-6-carbonyl)-1H-indole-3-carboxylicacid cyanomethyl-amide;5-(1,3,3-Trimethyl-6-aza-bicyclo[3.2.1]octane-6-carbonyl)-1H-indole-3-carboxylicacid benzylamide;5-(1,3,3-Trimethyl-6-aza-bicyclo[3.2.1]octane-6-carbonyl)-1H-indole-3-carboxylicacid dimethylamide;5-(1,3,3-Trimethyl-6-aza-bicyclo[3.2.1]octane-6-carbonyl)-1H-indole-3-carboxylicacid allylamide;5-(1,3,3-Trimethyl-6-aza-bicyclo[3.2.1]octane-6-carbonyl)-1H-indole-3-carboxylicacid (2-dimethylamino-ethyl)-methyl-amide;5-(1,3,3-Trimethyl-6-aza-bicyclo[3.2.1]octane-6-carbonyl)-1H-indole-3-carboxylicacid (2-methoxy-ethyl)-amide;5-(1,3,3-Trimethyl-6-aza-bicyclo[3.2.1]octane-6-carbonyl)-1H-indole-3-carboxylicacid 4-methoxy-benzylamide;5-(1,3,3-Trimethyl-6-aza-bicyclo[3.2.1]octane-6-carbonyl)-1H-indole-3-carboxylicacid (tetrahydro-furan-2-ylmethyl)-amide;[3-(2-Methoxymethyl-pyrrolidine-1-carbonyl)-1H-indol-5-yl]-(1,3,3-trimethyl-6-aza-bicyclo-[3.2.1]oct-6-yl)-methanone;[3-(2,6-Dimethyl-morpholine-4-carbonyl)-1H-indol-5-yl]-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone;5-(1,3,3-Trimethyl-6-aza-bicyclo[3.2.1]octane-6-carbonyl)-1H-indole-3-carboxylicacid (1,1-dioxo-tetrahydro-thiophen-3-yl)-amide;5-(1,3,3-Trimethyl-6-aza-bicyclo[3.2.1]octane-6-carbonyl)-1H-indole-3-carboxylicacid [3-(4-methyl-piperazin-1-yl)-propyl]-amide;5-(1,3,3-Trimethyl-6-aza-bicyclo[3.2.1]octane-6-carbonyl)-1H-indole-3-carboxylicacid 4-trifluoromethyl-benzylamide;5-(1,3,3-Trimethyl-6-aza-bicyclo[3.2.1]octane-6-carbonyl)-1H-indole-3-carboxylicacid (furan-2-ylmethyl)-amide;[3-(2,3,5,6-Tetrahydro-[1,2′]bipyrazinyl-4-carbonyl)-1H-indol-5-yl]-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone;5-(1,3,3-Trimethyl-6-aza-bicyclo[3.2.1]octane-6-carbonyl)-1H-indole-3-carboxylicacid (2H-tetrazol-5-ylmethyl)-amide;[3-(1,3,3-Trimethyl-6-aza-bicyclo[3.2.1]octane-6-carbonyl)-1H-indol-5-yl]-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone;3-{[5-(1,3,3-Trimethyl-6-aza-bicyclo[3.2.1]octane-6-carbonyl)-1H-indole-3-carbonyl]-amino}-propionicacid ethyl ester;5-(1,3,3-Trimethyl-6-aza-bicyclo[3.2.1]octane-6-carbonyl)-1H-indole-3-carboxylicacid (4-methoxy-phenyl)-amide;3-{[5-(1,3,3-Trimethyl-6-aza-bicyclo[3.2.1]octane-6-carbonyl)-1H-indole-3-carbonyl]-amino}-propionicacid; Azepan-1-yl-(1H-indol-5-yl)-methanone; 1H-Indole-5-carboxylic aciddibenzylamide; (3-Aza-bicyclo[3.2.2]non-3-yl)-(1H-indol-5-yl)-methanone;(4-Benzyl-piperidin-1-yl)-(1H-indol-5-yl)-methanone;8-(1H-Indole-5-carbonyl)-1-phenyl-1,3,8-triaza-spiro[4.5]decan-4-one;[4-(4-Chloro-phenyl)-4-hydroxy-piperidin-1-yl]-(1H-indol-5-yl)-methanone;1-[1-(1H-Indole-5-carbonyl)-piperidin-4-yl]-1,3-dihydro-benzoimidazol-2-one;(4-tert-Butyl-piperidin-1-yl)-(1H-indol-5-yl)-methanone;1-(1H-Indole-5-carbonyl)-4-phenyl-piperidine-4-carbonitrile;(1H-Indol-5-yl)-(4-phenyl-piperidin-1-yl)-methanone;(5-Benzyl-2,5-diaza-bicyclo[2.2.1]hept-2-yl)-(1H-indol-5-yl)-methanone;(1H-Indol-5-yl)-(4-pyrrolidin-1-yl-piperidin-1-yl)-methanone;1H-Indole-5-carboxylic acid(5-hydroxy-1,3,3-trimethyl-cyclohexylmethyl)-amide;1H-Indole-5carboxylic acid(3,4-dihydrospiro(1H-indene-1,4-piperidine)-amide;(3-Methanesulfonylmethyl-1H-indol-5-yl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone;(3-Dimethylaminomethyl-1H-indol-6-yl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone;1-{3-Acetyl-2-[5-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]octane-6-carbonyl)-1H-indol-3-yl]-2,3-dihydro-imidazol-1-yl}-ethanone;1-Ethyl-3-[5-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]octane-6-carbonyl)-1H-indol-3-yl]-pyrrolidine-2,5-dione;(3-Thiazol-2-yl-1H-indol-5-yl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone;(3-Iodo-1H-indol-5-yl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone;6-(1,3,3-Trimethyl-6-aza-bicyclo[3.2.1]octane-6-carbonyl)-1H-indole-3-carbonitrile;5-(1,3,3-Trimethyl-6-aza-bicyclo[3.2.1]octane-6-carbonyl)-1H-indole-3-carbonitrile;6-(1,3,3-Trimethyl-6-aza-bicyclo[3.2.1]octane-6-carbonyl)-1H-indole-3-carboxylicacid amide;[3-(2H-Tetrazol-5-yl)-1H-indol-6-yl]-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone;N-[3-(1,3,3-Trimethyl-6-aza-bicyclo[3.2.1]octane-6-carbonyl)-1H-indol-7-yl]-acetamide;(1-Benzenesulfonyl-1H-indol-5-yl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone;(1-Benzenesulfonyl-2-methyl-1H-indol-5-yl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone;(1-methyl-1H-indol-5-yl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone;(1-Benzyl-1H-indol-5-yl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone;[6-(1,3,3-Trimethyl-6-aza-bicyclo[3.2.1]octane-6-carbonyl)-indol-1-yl]-aceticacid ethyl ester;[1-(2-Ethoxy-ethyl)-1H-indol-6-yl]-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone;{1-[2-(2-Methoxy-ethoxy)-ethyl]-1H-indol-6-yl}-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone;3-[5-(1,3,3-Trimethyl-6-aza-bicyclo[3.2.1]octane-6-carbonyl)-indol-1-yl]-propionicacid ethyl ester;(1-Phenethyl-1H-indol-5-yl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone;[1-(Tetrahydro-furan-2-ylmethyl)-1H-indol-5-yl]-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone;2-[5-(1,3,3-Trimethyl-6-aza-bicyclo[3.2.1]octane-6-carbonyl)-indol-1-yl]-acetamide;[1-(4-Trifluoromethoxy-benzyl)-1H-indol-5-yl]-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone;3-[5-(1,3,3-Trimethyl-6-aza-bicyclo[3.2.1]octane-6-carbonyl)-indol-1-ylmethyl]-benzoicacid methyl ester; and4-[5-(1,3,3-Trimethyl-6-aza-bicyclo[3.2.1]octane-6-carbonyl)-indol-1-ylmethyl]-benzonitrile;or a salt thereof with a pharmaceutically acceptable acid or base, oroptical isomer or mixture of optical isomers, racemic mixture, ortautomeric forms thereof.
 92. A compound of formula (VIII):

wherein X is NR⁴, S or O; R¹ and R² independently are hydrogen, halo,cyano, trihalomethyl, C₁-C₆alkyl or C₁-C₆alkyloxy, wherein the alkylgroups independently are optionally substituted with one or more of R⁷;R³ is hydrogen, C₁-C₆alkyl, C₃-C₁₀cycloalkyl, C₁-C₆alkyloxy,C₁-C₆alkylthio, aryl, arylC₁-C₆alkyl, hetaryl or hetarylalkyl, whereinthe alkyl, cycloalkyl, aryl, hetaryl and hetarylalkyl groupsindependently are optionally substituted with one or more of R⁷; R⁴ ishydrogen, C₁-C₈alkyl, C₁-C₆alkyloxyC₁-C₆alkyl, aryl, hetaryl,hetarylC₁-C₆alkyl, arylC₁-C₆alkyl, arylC₁-C₆alkyloxyC₁-C₆alkyl,C₃-C₁₀cycloalkyl, C₃-C₁₀hetcycloalkyl, C₃-C₁₀cycloalkylC₁-C₆alkyl,C₁-C₆alkylcarboxyC₁-C₆alkyl wherein the alkyl, aryl, hetaryl, cycloalkyland hetcycloalkyl groups independently are optionally substituted withone or more of R⁷; R⁵ is hydrogen, and R⁶ is adamantyl optionallysubstituted with hydroxy, C₁-C₆alkyloxy, aryl, arylC₁-C₆alkyl, aryloxy,arylC₁-C₆alkyloxy, hetaryl, hetaryloxy or hetarylC₁-C₆alkyloxy whereinthe alkyl, aryl and hetaryl groups independently are optionallysubstituted with one or more of R⁷; or R⁵ and R⁶ are together with thenitrogen to which they are attached, forming a saturated or partiallysaturated cyclic, bicyclic or tricyclic ring system containing from 6 to10 carbon atoms and from 0 to 2 additional heteroatoms selected fromnitrogen, oxygen or sulphur, the ring system optionally beingsubstituted with at least one of C₁-C₆alkyl, aryl, hetaryl,arylC₁-C₆alkyl, hetarylalkyl, hydroxy, oxo, cyano, C₁-C₆alkyloxy,arylC₁-C₆alkyloxy, hetarylC₁-C₆alkyloxy, C₁-C₆alkyloxyC₁-C₆alkyl,C₁-C₆alkylcarbonyl, arylcarbonyl, hetarylcarbonyl,arylC₁-C₆alkylcarbonyl, hetarylC₁-C₆alkylcarbonyl, C₁-C₆alkylcarboxy,arylcarboxy or arylC₁-C₆alkylcarboxy wherein the alkyl and aryl groupsindependently are optionally substituted with one or more of R⁷; R⁷ areindependently hydrogen, halo, hydroxy, oxo, nitro, NR⁹R¹⁰, cyano, COOR⁸,CONR⁹R¹⁰, C₁-C₈alkyl, C₁-C₆alkyloxy, aryloxy, arylC₁-C₆alkyloxy,hetaryloxy or hetarylC₁-C₆alkyloxy; R⁸ is hydrogen, C₁-C₆alkyl, aryl,arylC₁-C₆alkyl, hetarylalkyl, wherein the alkyl, aryl and hetarylalkylgroups independently are optionally substituted with one or more of R⁷;R⁹ and R¹⁰ independently are hydrogen, C₁-C₈alkyl, C₃-C₁₀cycloalkyl,C₃-C₁₀hetcycloalkyl, C₃-C₁₀cycloalkylC₁-C₆alkyl, wherein the alkyl,cycloalkyl and hetcycloalkyl groups independently are optionallysubstituted with one or more of R⁷; or R⁹ and R¹⁰ together with thenitrogen to which they are attached, are forming a saturated orpartially saturated bicyclic or tricyclic ring system containing from 4to 10 carbon atoms and from 0 to 2 additional heteroatoms selected fromnitrogen or oxygen, the ring system optionally being substituted with atleast one of C₁-C₈alkyl, arylC₁-C₆alkyl, hetarylC₁-C₆alkyl, hydroxy,cyano, C₁-C₆alkyloxy, arylC₁-C₆alkyloxy, hetarylC₁-C₆alkyloxy,C₁-C₆alkyloxyC₁-C₆alkyl, C₁-C₆alkylcarbonyl, arylcarbonyl,hetarylcarbonyl, arylC₁-C₆alkylcarbonyl, hetarylC₁-C₆-alkylcarbonyl,C₁-C₆alkylcarboxy, arylcarboxy or arylC₁-C₆alkylcarboxy wherein thealkyl and aryl groups independently are optionally substituted with oneor more of R¹¹; R¹¹ is hydrogen, halo, oxo, hydroxy, C₁-C₆alkyl, aryl,arylC₁-C₆alkyl, hetaryl or hetarylalkyl; provided that hetcycloalkyl isnot 7-aza[2,2,1]bicycloheptane; or a salt thereof with apharmaceutically acceptable acid or base, or optical isomer or mixtureof optical isomers, racemic mixture, or tautomeric forms thereof.
 93. Acompound according to claim 92, wherein X is NR⁴, S or O; R¹ and R²independently are hydrogen, halo, cyano, trihalomethyl, C₁-C₆alkyl orC₁-C₆alkyloxy, wherein the alkyl groups independently are optionallysubstituted with one or more of R⁷; R³ is hydrogen, C₁-C₆alkyl,C₃-C₁₀cycloalkyl, C₁-C₆alkyloxy, C₁-C₆alkylthio, aryl, arylC₁-C₆alkyl,hetaryl or hetarylalkyl, wherein the alkyl, cycloalkyl, aryl, hetaryland hetarylalkyl groups independently are optionally substituted withone or more of R⁷; R⁴ is hydrogen, C₁-C₈alkyl, C₁-C₆alkyloxyC₁-C₆alkyl,aryl, hetaryl, arylC₁-C₆alkyl, arylC₁-C₆-alkyloxyC₁-C₆alkyl,C₃-C₁₀cycloalkyl, C₃-C₁₀hetcycloalkyl, C₃-C₁₀cycloalkylC₁-C₆alkyl,C₁-C₆-alkylcarboxyC₁-C₆alkyl wherein the alkyl, aryl, hetaryl,cycloalkyl and hetcycloalkyl groups independently are optionallysubstituted with one or more of R⁷; R⁵ is hydrogen, and R⁶ is adamantyloptionally substituted with hydroxy, C₁-C₆alkyloxy, aryl,arylC₁-C₆alkyl, aryloxy, arylC₁-C₆alkyloxy, hetaryl, hetaryloxy orhetarylC₁-C₆alkyloxy wherein the alkyl, aryl and hetaryl groupsindependently are optionally substituted with one or more of R⁷; or R⁵and R⁶ are together with the nitrogen to which they are attached,forming a saturated or partially saturated cyclic, bicyclic or tricyclicring system containing from 6 to 10 carbon atoms and from 0 to 2additional heteroatoms selected from nitrogen, oxygen or sulphur, thering system optionally being substituted with at least one ofC₁-C₆alkyl, aryl, hetaryl, arylC₁-C₆alkyl, hetarylalkyl, hydroxy, oxo,cyano, C₁-C₆alkyloxy, arylC₁-C₆alkyloxy, hetarylC₁-C₆alkyloxy,C₁-C₆alkyloxyC₁-C₆alkyl, C₁-C₆alkylcarbonyl, arylcarbonyl,hetarylcarbonyl, arylC₁-C₆alkylcarbonyl, hetarylC₁-C₆alkylcarbonyl,C₁-C₆alkylcarboxy, arylcarboxy or arylC₁-C₆alkylcarboxy wherein thealkyl and aryl groups independently are optionally substituted with oneor more of R⁷; R⁷ are independently hydrogen, halo, hydroxy, oxo, nitro,NR⁵R⁶, cyano, COOR⁸, CONR⁵R⁶, C₁-C₈alkyl, C₁-C₆alkyloxy, aryloxy orhetaryloxy; R⁸ is hydrogen, C₁-C₆alkyl, aryl, arylC₁-C₆alkyl,hetarylalkyl, wherein the alkyl, aryl and hetarylalkyl groupsindependently are optionally substituted with one or more of R⁷;provided that hetcycloalkyl is not 7-aza[2,2,1]bicycloheptane; or a saltthereof with a pharmaceutically acceptable acid or base, or opticalisomer or mixture of optical isomers, racemic mixture, or tautomericforms thereof.
 94. A compound according to claim 92, wherein X is NR⁴ orS.
 95. A compound according to claim 92, wherein R¹ and R² independentlyare hydrogen, halo, trihalomethyl or C₁-C₆alkyl, wherein the alkyl groupis optionally substituted with one or more of R⁷ wherein R⁷.
 96. Acompound according to claim 92, wherein R³ is hydrogen, C₁-C₆alkyl,aryl, arylC₁-C₆-alkyl, hetaryl or hetarylalkyl, wherein the alkyl,cycloalkyl, aryl, hetaryl and hetarylalkyl groups independently areoptionally substituted with one or more of R⁷ wherein R⁷.
 97. A compoundaccording to claim 92, wherein R⁴ is hydrogen, C₁-C₈alkyl, aryl,hetaryl, hetarylC₁-C₆alkyl, arylC₁-C₆alkyl, wherein the alkyl, aryl,hetaryl, groups independently are optionally substituted with one ormore of R⁷ wherein R⁷.
 98. A compound according to claim 92, wherein R⁵and R⁶ are together with the nitrogen to which they are attached,forming a saturated or partially saturated cyclic, bicyclic or tricyclicring system containing from 6 to 10 carbon atoms and from 0 to 2additional heteroatoms selected from nitrogen, oxygen or sulphur, thering system optionally being substituted with at least one ofC₁-C₆alkyl, aryl, hetaryl, arylC₁-C₆alkyl, hetarylalkyl, hydroxy, oxo,cyano, C₁-C₆alkyloxy, arylC₁-C₆alkyloxy, hetarylC₁-C₆alkyloxy,C₁-C₆alkyloxyC₁-C₆alkyl, C₁-C₆alkylcarbonyl, arylcarbonyl,hetarylcarbonyl, arylC₁-C₆alkylcarbonyl, hetarylC₁-C₆alkylcarbonyl,C₁-C₆alkylcarboxy, arylcarboxy or arylC₁-C₆alkylcarboxy wherein thealkyl and aryl groups independently are optionally substituted with oneor more of R⁷.
 99. A compound according to claim 92, which is selectedfrom:(4-Methyl-2-phenyl-thiazol-5-yl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone;(2,4-Dimethyl-thiazol-5-yl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone;and(4-Methyl-2-pyrazin-2-yl-thiazol-5-yl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone;or a salt thereof with a pharmaceutically acceptable acid or base, oroptical isomer or mixture of optical isomers, racemic mixture, a prodrugthereof, or tautomeric forms thereof.
 100. A compound according to claim92, selected from the group consisting of:[4-Methyl-2-(4-trifluoromethyl-phenyl)-thiazol-5-yl]-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone;(3-Aza-bicyclo[3.2.2]non-3-yl)-(2,4-dimethyl-thiazol-5-yl)-methanone;(1H-Imidazol-4-yl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone;(3-Aza-bicyclo[3.2.2]non-3-yl)-(4-methyl-2-phenyl-thiazol-5-yl)-methanone;2,4-Dimethyl-thiazole-5-carboxylic acid cycloheptylamide;Azepan-1-yl-(2,4-dimethyl-thiazol-5-yl)-methanone;2,4-Dimethyl-thiazole-5-carboxylic acid adamantan-1-ylamide;(3-Aza-bicyclo[3.2.2]non-3-yl)-(1H-imidazol-4-yl)-methanone;2,4-Dimethyl-thiazole-5-carboxylic acid(3-hydroxy-adamantan-1-yl)-amide;(1-Methyl-1H-imidazol-4-yl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone;[1-(6-Methyl-pyridin-2-yl)-1H-imidazol-4-yl]-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone;and[1-(4-Chloro-benzyl)-5-methyl-1H-imidazol-4-yl]-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone;or a salt thereof with a pharmaceutically acceptable acid or base, oroptical isomer or mixture of optical isomers, racemic mixture, ortautomeric forms thereof.
 101. A compound according to any one of claims28, 38, 39, 48, 49, 50, 51, 55, 56, 57, 58, 67, 68, 69, 70, 81, 82, 83,90, 91, 92, 99 or 100, which is an agent useful for the treatment,prevention and/or prophylaxis of any conditions, disorders and diseaseswherein a modulation or an inhibition of the activity of 11βHSD1 isbeneficial.
 102. A compound according to any one of claims 28, 38, 39,48, 49, 50, 51, 55, 56, 57, 58, 67, 68, 69, 70, 81, 82, 83, 90, 91, 92,99 or 100, which is an agent useful for the treatment, prevention and/orprophylaxis of any conditions, disorders and diseases that areinfluenced by intracellular glucocorticoid levels.
 103. A compoundaccording to claim 101 or 102, which is an agent useful for thetreatment, prevention and/or prophylaxis of conditions, disorders ordiseases selected from the group consisting of the metabolic syndrome,insulin resistance, dyslipidemia, hypertension and obesity.
 104. Acompound according to claim 101 or 102, which is an agent useful for thetreatment, prevention and/or prophylaxis of type 2 diabetes, impairedglucose tolerance (IGT), impaired fasting glucose (IFG).
 105. A compoundaccording to claim 101 or 102, which is an agent useful for the delayingor prevention of the progression from IGT into type 2 diabetes.
 106. Acompound according to claim 101 or 102, which is an agent useful fordelaying or prevention of the progression of the metabolic syndrome intotype 2 diabetes.
 107. A compound according to claim 101 or 102, which isan agent useful for the treatment, prevention and/or prophylaxis ofadverse effects of glucocorticoid receptor agonist treatment or therapy.108. A pharmaceutical composition comprising, as an active ingredient,at least one compound according to any one of claims 28, 38, 39, 48, 49,50, 51, 55, 56, 57, 58, 67, 68, 69, 70, 81, 82, 83, 90, 91, 92, 99 or100, together with one or more pharmaceutically acceptable carriers orexcipients.
 109. The pharmaceutical composition according to claim 108which is for oral, nasal, buccal, transdermal, pulmonal or parenteraladministration.
 110. The pharmaceutical composition according to claim108 or 109, in unit dosage form, comprising from 0.05 mg to 2000 mg/day,from 0.1 mg to 1000 mg or from 0.5 mg to 500 mg per day of the compound.111. A method for the treatment, prevention and/or prophylaxis of anyconditions, disorders or diseases wherein a modulation or an inhibitionof the activity of 11βHSD1 is beneficial, the method comprisingadministering to a subject in need thereof an effective amount of acompound according to any one of claims 28, 38, 39, 48, 49, 50, 51, 55,56, 57, 58, 67, 68, 69, 70, 81, 82, 83, 90, 91, 92, 99 or
 100. 112. Themethod according to claim 111, wherein the conditions, disorders ordiseases are selected from the group consisting of the metabolicsyndrome, insulin resistance, dyslipidemia, hypertension and obesity.